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FDA 510(k)

GLOUCH(TM) PATIENT EXAMINATION GLOVES

K-Number: K891833 · 1989-08-22

ApplicantVadax, Inc.
Decision Date1989-08-22
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLOUCH(TM) PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Vadax, Inc.. It received FDA 510(k) clearance on 1989-08-22 under 510(k) number K891833. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOUCH(TM) PATIENT EXAMINATION GLOVES?

GLOUCH(TM) PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-22. The listed applicant is Vadax, Inc.. The 510(k) number is K891833.

When did GLOUCH(TM) PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

GLOUCH(TM) PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-22, under 510(k) number K891833.

Who is the listed applicant for GLOUCH(TM) PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Vadax, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLOUCH(TM) PATIENT EXAMINATION GLOVES?

The FDA product code for GLOUCH(TM) PATIENT EXAMINATION GLOVES is LZA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LZA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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