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FDA 510(k)

TAK, VINYL PATIENT EXAMINATION GLOVES

K-Number: K891645 · 1989-04-25

Decision Date1989-04-25
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAK, VINYL PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Tak Ent., Inc.. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K891645. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAK, VINYL PATIENT EXAMINATION GLOVES?

TAK, VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Tak Ent., Inc.. The 510(k) number is K891645.

When did TAK, VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

TAK, VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-04-25, under 510(k) number K891645.

Who is the listed applicant for TAK, VINYL PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for TAK, VINYL PATIENT EXAMINATION GLOVES?

The FDA product code for TAK, VINYL PATIENT EXAMINATION GLOVES is LYZ.

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 Tak Ent., Inc. 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: LYZ)

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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