POLARIS DIAL-A-DATE CONTACT LENS CASE

K120904 · Reliance Design & Manufacture Corp. · LRX · Nov 26, 2012 · Ophthalmic

Device Facts

• Record ID: K120904
• Device Name: POLARIS DIAL-A-DATE CONTACT LENS CASE
• Applicant: Reliance Design & Manufacture Corp.
• Product Code: LRX · Ophthalmic
• Decision Date: Nov 26, 2012
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 886.5928
• Device Class: Class 2

Intended Use

The Polaris Dial-a-Date Contact Lens Case is intended for the storage of soft (hydrophilic), rigid gas permeable, and/or hard contact lenses. Used for storage during chemical disinfection only. Not for use during heat disinfection.

Device Story

Polaris Dial-a-Date is a manual contact lens storage case. Device consists of a molded dual-compartment base and two screw-down lids. Each lid features a manual rotating dial marked with numbers (0-3 and 0-9) to allow users to set a reminder for lens replacement. Lenses are immersed in chemical disinfection solution within the compartments. Device is for OTC use by contact lens wearers. The outer lids and dials do not contact the lens care solution. The device provides a physical mechanism for tracking lens replacement schedules, aiding patient compliance with recommended replacement intervals.

Clinical Evidence

Bench testing only. Biocompatibility testing performed per ISO 10993-5 (cytotoxicity), ISO 10993-10 (skin sensitization and ocular irritation), and ISO 10993-11 (systemic toxicity) showed no adverse effects. Leakage testing conducted on 192 units (filled to 2/3 capacity, inverted for 15 minutes, repeated 3 times) demonstrated zero leakage.

Technological Characteristics

Materials: Polyolefin (>95%) and mixture (<5%). Dimensions: 69.50mm x 33.50mm x 18.91mm. Volume: 4.4 ml per side. Principle: Manual storage container with integrated mechanical dial for replacement tracking. Non-powered. Standalone device.

Indications for Use

Indicated for storage of soft (hydrophilic), rigid gas permeable, and hard contact lenses during chemical disinfection. Not for use with heat disinfection.

Regulatory Classification

Identification

A soft (hydrophilic) contact lens care product is a device intended for use in the cleaning, rinsing, disinfecting, lubricating/rewetting, or storing of a soft (hydrophilic) contact lens. This includes all solutions and tablets used together with soft (hydrophilic) contact lenses and heat disinfecting units intended to disinfect a soft (hydrophilic) contact lens by means of heat.

Special Controls

*Classification.* Class II (Special Controls) Guidance Document: “Guidance for Industry Premarket Notification (510(k)) Guidance Document for Contact Lens Care Products.”

Predicate Devices

• Polaris Contact Lens Case (K093377)

Submission Summary (Full Text)

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K120904

Image /page/0/Picture/1 description: The image shows the word "RELIANCE" in bold, sans-serif font. To the left of the word is a logo that appears to be an eagle head inside of a square with a check mark. The logo and the word are both in black. The background is white.

NOV 26 2012 1

# 510(k) Summary

(per 21 CFR 807.92)

# Submission Correspondent

Emergo Group, Inc. www.emergogroup.com/

## Address

611 West Fifth Street Third Floor Austin, TX 78701 USA

# Phone

[phone] Fax [phone]

# Contact

Caroline Tontini to [e-mail]

### Submission Sponsor

Reliance Design & Manufacture Corp. No.19, Lane 166, Yanhe St., Yongkang Dist. Tainan City 71082, Taiwan R.O.C

FDA Establishment Registration #: 3008388282

# Date Prepared

February 10th, 2012

# Trade Name

Polaris Dial-a-Date Contact Lens Case

# Classification Name

Soft (hydrophilic) contact lens care products

# Regulation Number 886.5928

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Product Code LRX

Classification Panel Ophthalmic Devices

Device Class Class 2

## Predicate Devices

Polaris Contact Lens Case (K093377) from Reliance Design & Manufacture Corp.

#### Intended Use

The Polaris Dial-a-Date Contact Lens Case is intended for the storage of soft (hydrophilic), rigid gas permeable, and/or hard contact lenses. Used for storage during chemical disinfection only. Not for use during heat disinfection.

#### Device Description

The Polaris Dial-a-Date contact lens case is a device for the storage of soft (hydrophilic) and rigid gas permeable contact lenses. Contact lenses can be fully immersed into the chamber and accommodates all lenses currently being sold in the market. The contact lens case consists of a molded dual compartment bottom base and two screwdown lids. The bottom of each compartment is marked with L (left) and R (right). The lids are also labeled with L (left) and R (right), and include a dial with molded-in numbers from 0 to 3 and 0 to 9, respectively. The outer lids are colored to make the molded-in numbers of the dials visible at the 'dialed position'. The dials can be incrementally rotated to let the user set reminders (i.e. day of the month to replace the contact lenses).

The outer lids and number dials do not come into contact with the lens care solution.

Image /page/1/Picture/12 description: The image shows an exploded view of a contact lens case and its components. The case itself is a double-sided container, with two circular depressions for holding the lenses. Above each side of the case, there is a lens and a corresponding cap, with dashed lines indicating the alignment and assembly order of the components. The image illustrates how the lens and cap fit together into the case.

Figure 5A Exploded View of the lens case illustrating the coloring of the Outer Lid

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K120904

Image /page/2/Picture/1 description: The image shows the word "RELIANCE" in bold, black letters. To the left of the word is a logo that features a white bird head inside of a black square. A black wing extends from the square. The logo and the word are aligned horizontally.

### Comparison of Technological Characteristics

The following table compares the Polaris Dial-a-Date to the POLARIS (201) with respect to intended use, technological characteristics and principles of operation.

| Table 5A – Comparison of Characteristics | | |
|------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Manufacturer | Reliance Design & Manufacture Corp. | Reliance Design & Manufacture Corp. |
| Product Name | POLARIS (201) Contact Lens Case | Polaris Dial-a-Date (202)<br>Contact Lens Case |
| 510(k) Number | K093377 | Pending |
| Classification<br>Advisory<br>Committee | Ophthalmic | Ophthalmic |
| Product Code | LRX | LRX |
| Regulation # | 886.5928 | 886.5928 |
| Class | 2 | 2 |
| Intended Use | For storage of soft (hydrophilic), rigid<br>gas permeable, and hard contact<br>lenses.<br>Use for storage during chemical<br>disinfection only. Not for use during<br>heat disinfection. | For storage of soft (hydrophilic), rigid<br>gas permeable, and/or hard contact<br>lenses.<br>Use for storage during chemical<br>disinfection only. Not for use during heat<br>disinfection. |
| Composition (%) | - Polyolefin > 95%<br>- Mixture < 5% | - Polyolefin > 95%<br>- Mixture < 5% |
| Size | Length: 67.97mm<br>Width: 31.97mm<br>Height: 21.50mm | Length: 69.50mm<br>Width: 33.50mm<br>Height: 18.91 |
| Volume | 3.0 ml each side | 4.4 ml each side |
| Number of Outer<br>Lid Colors | Four (4) | Four (4) |

## Table 5A - Comparison of Characteristics

## Summary of Differences

The Polaris Dial-a-Date Contact Lens Case differs from its predicate device POLARIS (201) in some aspects that however do not affect its safety or performance. The differences are as follows:

- a) the Polaris Dial-a-Date (202) has a moveable part on the top lid to set a reminder while the predicate device POLARIS (201) has a plain top
- b) the dimensions length, height and width differ slightly
- c) the compartment volume is larger: 4.4 ml vs. 3.0 ml

## Summary of Non-Clinical Data Submitted

The following testing has been performed to support substantial equivalence:

- · Biocompatibility Testing according to the applicable standards, as described in Section 15 Biocompatibility
- Leakage Testing, as described in Section 18 Performance Testing Bench Studies

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K120904

Image /page/3/Picture/1 description: The image shows the word "RELIANCE" in bold, black letters. To the left of the word is a black square with a white bird-like figure inside. The bird figure appears to be flying or diving. The logo is simple and modern.

#### Biocompatibility Testing

The Polaris Dial-a-Date contact lens case has been evaluated for biocompatibility in accordance with Part 10993 of the ISO Standard tests, which include:

- . ISO 10993-5:1999, Biological evaluation of medical devices -- Part 5: Tests for In Vitro Cytotoxicity.
The test article did not induce cytotoxic effects and did not inhibit cell proliferation after being exposed for 24 to 48 hours in L929 colorectal carcinoma cells

- ISO 10993-10:2006, Biological evaluation of medical devices Part 10: Tests for . irritation and delayed-type hypersensitivity (Skin Sensitization). Under the conditions of this study, the test article extracted by Sodium Chloride 0.9% Inj. showed no evidence of causing delayed dermal contact sensitization in guinea pigs.
- . ISO 10993-10:2006, Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (Ocular Irritation). All grades of ocular irritation calculated by maximum average score were zero. Based on the conditions and results of the study, the test article extract administered to NZW rabbits by ocular instillation did not cause any observable irritation response in vivo. All data generated from this study will provide as safety reference for human exposure.
- . ISO 10993-11:2006, Biological evaluation of medical devices -- Part 11: Tests for systemic toxicity.

Under the conditions of this study, there was no mortality or evidence of systemic toxicity from the test article extract injected into ICR mice. All data generated from this study will provide as safety criteria for human exposure.

- . ISO 10993-12:2007, Biological evaluation of medical devices -- Part 12: Sample preparation and reference materials. (Biocompatibility).
#### Leakage Testing

Production units of the Polaris Dial-a-Date contact lens case have undergone leakage testing

The Polaris Dial-a-Date contact lens case was tested for leakage following a written test protocol. 192 combinations of different tops and bottoms were filled to 2/3 with liquid. Each set was turned upside down for 15 minutes and the tests were repeated 3 times. None of the tested lens cases showed any leakage and all of the Leakage Tests passed successfully. The results were documented

The Polaris Dial-a-Date Contact Lens Case complies with the voluntary standards as detailed in Section 9 Declarations of Conformity and Summary Reports of this submission.

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K120904

Image /page/4/Picture/1 description: The image shows the word "RELIANCE" in bold, black letters. To the left of the word is a black graphic that appears to be a stylized bird or eagle. The text is the main focus of the image, and the graphic serves as a visual element associated with the brand or company name.

# Safety and Effectiveness

By definition, a device is substantially equivalent to a predicate device when the device has the same intended use and the same technological characteristics as the previously cleared predicate device, or has the same intended use and different technological characteristics, and it can be demonstrated that the device is substantially equivalent to the predicate device, and that the new device does not raise different questions regarding its safety and effectiveness as compared to the predicate device.

It has been shown in this 510(k) submission that the differences between the Polaris Diala-Date Contact Lens Case and the predicate device do not raise any questions regarding its safety and effectiveness. The Polaris Dial-a-Date Contact Lens Case, as designed and manufactured, therefore is determined to be substantially equivalent to the referenced predicate device.

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Image /page/5/Picture/0 description: The image is a circular logo for the Department of Health & Human Services - USA. The logo features the department's name in a circular arrangement around the perimeter. In the center is a stylized symbol, possibly representing a bird or a flame, composed of three curved lines.

#### DEPARTMENT OF HEALTH & HUMAN SERVICES

November 26, 2012

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002

NOV 2 6 2012

Reliance Design and Manufacture Corp. % Ms. Caroline Tontini International Project Manager Emergo Group, Incorporated 611 West 5th Street, Third Floor Austin, TX 78701

K120904 Re:

> Trade/Device Name: Polaris Dial-a-Date Contact Lens Case Regulation Number: 21 CFR 886.5928 Regulation Name: Soft (hydrophilic) Contact Lens Care Products Regulatory Class: Class II Product Code: LRX Dated: October 22, 2012 Received: October 31, 2012

Dear Ms. Tontini:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must

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comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours.

**Kesia Y. Alexander**

Malvina B. Eydelman, M.D. Director Division of Ophthalmic and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# Indications for Use Statement

510(k) Number (if known): K120904

Device Name: Polaris "Dial-A-Date" Contact Lens Case

Indications for Use:

Polaris 'Dial-A-Date' is a contact lens case for storage of soft (hydrophilic), rigid gas permeable, and hard contact lenses. Use for storage during chemical disinfection only.

Not for use during heat disinfection.

Prescription Use (Part 21 CFR 801 Subpart D) AND/OR

Over-The-Counter Use X (21 CFR 801 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

MARC ROBBOY

sion Sign-O Division of Ophthalmic and Ear, Nose and Throat Devices 510(k) Number