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FDA 510(k)

UNIJECT EXAMINATION GLOVES

K-Number: K970191 · 1997-07-03

Decision Date1997-07-03
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIJECT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Uniject Gloves , Ltd.. It received FDA 510(k) clearance on 1997-07-03 under 510(k) number K970191. 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 UNIJECT EXAMINATION GLOVES?

UNIJECT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Uniject Gloves , Ltd.. The 510(k) number is K970191.

When did UNIJECT EXAMINATION GLOVES receive FDA 510(k) clearance?

UNIJECT EXAMINATION GLOVES received FDA 510(k) clearance on 1997-07-03, under 510(k) number K970191.

Who is the listed applicant for UNIJECT EXAMINATION GLOVES?

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

What is the FDA product code for UNIJECT EXAMINATION GLOVES?

The FDA product code for UNIJECT EXAMINATION GLOVES is LYY.

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.

Other records listing Uniject Gloves , Ltd. as applicant

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: LYY)

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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