FDA 510(k)

ANTELOPE BRAND PATIENT EXAMINATION GLOVES

K-Number: K892781 · 1989-09-21

Decision Date1989-09-21

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ANTELOPE BRAND PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning-Usa Corp.. It received FDA 510(k) clearance on 1989-09-21 under 510(k) number K892781. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTELOPE BRAND PATIENT EXAMINATION GLOVES?

ANTELOPE BRAND PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-09-21. The listed applicant is Liaoning-Usa Corp.. The 510(k) number is K892781.

When did ANTELOPE BRAND PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

ANTELOPE BRAND PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-09-21, under 510(k) number K892781.

Who is the listed applicant for ANTELOPE BRAND PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Liaoning-Usa Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTELOPE BRAND PATIENT EXAMINATION GLOVES?

The FDA product code for ANTELOPE BRAND PATIENT EXAMINATION GLOVES is LYY.

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Other records listing Liaoning-Usa Corp. as applicant

K911921DISPOSABLE ISOLATION GOWN K905487VARIOUS TYPES OF STETHOSCOPES K910623GAUZE SPONGES ABSORBENT GAUZE ROLLS K902625CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT K892774PATIENT EXAMINATION GLOVES

Related Devices (Code: LYY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.