MANAN VS ACCESS NEEDLE/SET

K980372 · Medical Device Technologies, Inc. · FGE · Apr 27, 1998 · Gastroenterology, Urology

Device Facts

• Record ID: K980372
• Device Name: MANAN VS ACCESS NEEDLE/SET
• Applicant: Medical Device Technologies, Inc.
• Product Code: FGE · Gastroenterology, Urology
• Decision Date: Apr 27, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 876.5010
• Device Class: Class 2

Intended Use

The Manan™ VS Access Needle/Set is intended for the introduction of a .038" guidewire used in abscess, biliary, nephrostomy, and other fluid collection drainage procedures.

Device Story

The Manan™ VS Access Needle/Set is a medical device used by clinicians to facilitate the introduction of a .038" guidewire into a patient. It is utilized during abscess, biliary, nephrostomy, and other fluid collection drainage procedures. The device functions as an access tool, allowing the physician to establish a pathway for subsequent drainage equipment. By enabling precise guidewire placement, the device assists in the clinical management of fluid collections, potentially improving procedural efficiency and patient outcomes during minimally invasive drainage interventions.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

The device is an access needle/set designed for .038" guidewire introduction. It is a mechanical, non-powered device. No specific materials, software, or energy sources are described.

Indications for Use

Indicated for patients requiring abscess, biliary, nephrostomy, or other fluid collection drainage procedures involving the introduction of a .038" guidewire.

Regulatory Classification

Identification

A biliary catheter and accessories is a tubular flexible device used for temporary or prolonged drainage of the biliary tract, for splinting of the bile duct during healing, or for preventing stricture of the bile duct. This generic type of device may include a bile collecting bag that is attached to the biliary catheter by a connector and fastened to the patient with a strap.

Special Controls

*Classification.* Class II (special controls). The device, when it is a bile collecting bag or a surgical biliary catheter that does not include a balloon component, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.

Predicate Devices

• V.S. Access Needle/Set (K963767)

Submission Summary (Full Text)

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Image /page/0/Picture/0 description: The image shows the logo for MDTECH MEDICAL DEVICE TECHNOLOGIES INC. The logo is in white text on a black background. The letters "MDTECH" are in a large, bold font, and the words "MEDICAL DEVICE TECHNOLOGIES INC" are in a smaller font below the letters.

# APR 27 1998

K980372

Pint

45-310 S.W. 35th Terrace Gainesville, Florida 32608 TEL: [phone] FAX: [phone]

#### 510(k) SUMMARY

APPLICANT:

Medical Device Technologies, Inc. 4445-310 SW 35th Terrace Gainesville, FL 32608

CONTACT:

Karl Swartz Quality Assurance Manager

TELEPHONE:

[phone] fax [phone]

TRADE NAMES:

Guidewire introduction needle

Manan™ VS Access Needle/Set

§878-4200 - Introduction/Drainage Catheter and Accessories

CLASSIFICATION NAME:

#### SUBSTANTIAL EQUIVALENCE:

COMMON NAME:

| Company Name | Product Name | 510(k) No. |
|------------------------|------------------------|------------|
| Manan Medical Products | V.S. Access Needle/Set | K963767 |

### DESCRIPTION OF DEVICE:

The Manan™ VS Access Needle/Set is intended for the introduction of a .038" guidewire used in abscess, biliary, nephrostomy, and other fluid collection drainage procedures.

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Image /page/1/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized depiction of an eagle with its wings spread, rendered in black. The words "DEPARTMENT OF HEALTH &" are vertically oriented along the left side of the logo. The words "HUMAN SERVICES" are vertically oriented along the right side of the logo.

- L

DEPARTMENT OF HEALTH & HUMAN SERVICES

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

## APR 2 7 1998

Mr. Karl Swartz Quality Assurance Manager Medical Device Technologies, Inc. 4445 S.W. 35th Terrace Gainesville, FL 32608

Re: K980372 Manan V.S. Access Needle/Set Dated: April 16, 1998 Received: April 17, 1998 Regulatory Class: II 21 CFR \$876.5010/Procode: 78 FGE

Dear Mr. Swartz:

We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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.

If your device is classified (see above) into either class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (OS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its Internet address "http://www.fda.gov/cdrh/dsmaldsmamain.html".

Sincerely yours,

Lillian Yin, Ph.D.

Director, Division of Reproductive, Abdominal, Ear, Nose and Throat and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Image /page/2/Picture/0 description: The image shows the logo for MDTECH MEDICAL DEVICE TECHNOLOGIES INC. The logo is in white text on a black background. The letters MDTECH are in a bold, sans-serif font, and the words MEDICAL DEVICE TECHNOLOGIES INC are in a smaller, sans-serif font below the letters MDTECH.

4445-310 S.W. 35th Terrace Gainesville, Florida 32608 TEL: [phone] FAX: [phone]

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510(k) Number (if known):

Device Name: Manan™ VS Access Needle/Set

Indications for Use:

The Manan™ VS Access Needle/Set is intended for the introduction of a .038" guidewire used in abscess, biliary, nephrostomy, and other fluid collection drainage procedures.

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

Concurrence of CDRH, Office of Device Evaluation (ODE)

Robert D. Satting/
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number K980372

OR

Prescription Use_ (Per 21 CFR 801.109)

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Over-The-Counter Use_

(Optional Format 1-2-96)