LOW PROTEIN LATEX EXAMINATION GLOVES

K970222 · Kossan Latex Industries(M)Sdn Bhd · LYY · Jun 24, 1997 · General Hospital

Device Facts

• Record ID: K970222
• Device Name: LOW PROTEIN LATEX EXAMINATION GLOVES
• Applicant: Kossan Latex Industries(M)Sdn Bhd
• Product Code: LYY · General Hospital
• Decision Date: Jun 24, 1997
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 880.6250
• Device Class: Class 1

Intended Use

A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand and finger to prevent contamination between patient and examiner.

Device Story

Disposable latex examination glove; intended for use by healthcare professionals to provide a protective barrier between examiner and patient. Device functions as a physical barrier to prevent cross-contamination. Used in clinical or medical settings. No electronic, software, or algorithmic components. Benefit is reduction of infection transmission risk during patient examinations.

Clinical Evidence

No clinical data provided; device is a standard patient examination glove.

Technological Characteristics

Powdered latex examination glove. Material: Natural rubber latex. Form factor: Disposable hand-worn barrier. No electronic components, software, or energy sources.

Indications for Use

Indicated for use as a disposable medical glove worn by examiners to prevent cross-contamination between patient and examiner. Suitable for general patient examination settings.

Regulatory Classification

Identification

A non-powdered patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. A non-powdered patient examination glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing.

Submission Summary (Full Text)

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DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
Food and Drug Administration
9200 Corporate Boulevard
Rockville MD 20850

Mr. Lim Kuang Sia
Kossan Latex Industries (M) Snd. Bhd.
Lot 16632, 5 1/4 Mile, Jalan Meru, 40150 Klang, Selangor
MALAYSIA

JUN 24 1997

Re: K970222
Trade Name: Powdered Latex Examination Gloves With Protein Content Labeling Claim
Regulatory Class: I
Product Code: LYY
Dated: May 20, 1997
Received: May 22, 1997

Dear Mr. Sia:

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 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 Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP 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

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Page 2 - Mr. Sia

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 at [phone].

Sincerely yours,

Timothy A. Ulatowski
Director
Division of Dental, Infection Control and General Hospital Devices
Office of Device Evaluation
Center for Devices and Radiological Health

Enclosure

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Page 17 of

510(k) Number (if known): K970222

Device Name: Water Reminiscence Glove with Protein Content Labeling Claim

Indications For Use:

A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand and finger to prevent contamination between patient and examiner.

(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 Dental, Infection Control,
and General Hospital Devices
(OK) Number K970222

Prescription Use
(Per 21 CFR 801.109)

OK

Over-The-Counter Use ☑

(Optional Format 1-2-96)