FIBER OPTIC ENDOILLUMINATION PROBE

K982462 · Microvision, Inc. · FFS · Sep 14, 1998 · Gastroenterology, Urology

Device Facts

• Record ID: K982462
• Device Name: FIBER OPTIC ENDOILLUMINATION PROBE
• Applicant: Microvision, Inc.
• Product Code: FFS · Gastroenterology, Urology
• Decision Date: Sep 14, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 876.1500
• Device Class: Class 2

Intended Use

The Fiber Optic Endoillumination Probe is indicated for intraocular illumination in vitreoretinal surgery.

Device Story

The Fiber Optic Endoillumination Probe provides intraocular illumination during vitreoretinal surgery. The device consists of a flexible optical fiber threaded through an illumination probe. Light is transmitted from an external source through the fiber to the interior of the eye. The device is used by surgeons in an operating room setting to improve visualization of the surgical field. It is a passive optical instrument; it does not perform automated analysis or processing.

Clinical Evidence

No clinical data. Substantial equivalence is based on technological and operational characteristics.

Technological Characteristics

Fiber optic probe for intraocular illumination. Materials: PMMA, fluoropolymer, and medical-grade surgical stainless steel. Sterilization: Validated ETO. Packaging: Heat-sealed Tyvek.

Indications for Use

Indicated for intraocular illumination in patients undergoing vitreoretinal surgery.

Regulatory Classification

Identification

An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

Special Controls

*Classification* —(1)*Class II (special controls).* The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.

Predicate Devices

• Infinitech, Inc. Fiber Optic Probe (K870942)

Submission Summary (Full Text)

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### SEP 1 4 1998

510(k) Summary Fiber Optic Endoillumination Probe (per 21 CFR 807.92)

K982462

#### SUBMITTER NAME AND ADDRESS 1.

MicroVision, Inc. 34 Folly Mill Road, Suite 200 P.O. Box 1651 Seabrook, NH 03874-1651

Leonard Kastrilevich, President Contact Person: Telephone: [phone] ← -

Date Prepared: July 13, 1998

#### 2. DEVICE NAME

Fiber Probe Trade Name: Fiber Optic Endoillumination Probe Proprietary Name: Light, Surgical, Fiberoptic Classification name:

#### 3. PREDICATE DEVICE

Infinitech, Inc. Fiber Optic Probe (K870942)

#### 4. DEVICE DESCRIPTION

The Fiber Optic Endoillumination Probe is provides intraocular illumination. The light is transmitted from the source to the inside of the eye through a flexible optical fiber, which has been threaded through an illumination probe.

#### 5. INTENDED USE

The Fiber Optic Endoillumination Probe is indicated for intraocular illumination in vitreoretinal surgery.

#### 6. BASIS FOR SUBSTANTIAL EQUIVALENCE

Operational and technological characteristics form the basis for the determination of substantial equivalence of the Fiber Optic Endoillumination Probe with legally marketed predicate devices. Information supplied in this premarket notification includes descriptive information about the intended use, operation, and technological characteristics.

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### COMPARISON TABLE

.

| Comparison Criteria | MicroVision, Inc.<br>Fiber Optic<br>Endoillumination Probe | Infinitech, Inc.<br>Fiber Optic<br>Probe |
|-------------------------------------------------------------------------------------------------------------|------------------------------------------------------------|------------------------------------------|
| Device Type: Fiber Optic<br>Probe | Yes | Yes |
| Indication: Intraocular<br>illumination in vitreoretinal<br>surgery | Yes | Yes |
| Patient Contact Materials:<br>PMMA and fluoropolymer<br>fiber and medical grade<br>Surgical stainless steel | Yes | Yes |
| Sterilitzation Method | Validated ETO | Not Known |
| Packaging | Validated Heat Sealed<br>Tyvek | Not Known |

1. September 19.

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

SEP 1 4 1998

Mr. Leonard Kastrilevich President Microvision, Inc. 34 Folly Mill Road, Suite 200 P.O. Box 1651 Seabrook, New Hampshire 03874-1651

Re: K982462

Trade Name: Fiber Optic Endoillumination Probe Regulatory Class: II Product Code: FFS Dated: July 13, 1998 Received: July 15, 1998

Dear Mr. Kastrilevich:

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 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). 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 II (Special Controls) or 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 (QS) 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 531 through 542 of the Act for devices

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Page 2 - Mr. Leonard Kastrilevich

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/dsma/dsmamain.html".

Sincerely yours,

Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# 510(k) Number (if known):

## Device Name: Fiber Optic Endoillumination Probe

## Indication For Use:

ﺎ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤ

(Per 21 CFR 801.109)

Fiber Optic Endoillumination Probe is indicated for intraocular illumination in vitreoretinal surgery.

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

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off)
Division of General Restorative Devices
510(k) Number 14982462

Prescription Use X OR

Over-The-Counter Use

OR