GLOUCH(TM) PATIENT EXAMINATION GLOVES
K-Number: K891833 · 1989-08-22
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement