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FDA 510(k)

VINYL PATIENT EXAMINATION GLOVE

K-Number: K890986 · 1989-04-04

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

Device Summary

VINYL PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Precious Mountain Ent. Corp.. It received FDA 510(k) clearance on 1989-04-04 under 510(k) number K890986. 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 VINYL PATIENT EXAMINATION GLOVE?

VINYL PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1989-04-04. The listed applicant is Precious Mountain Ent. Corp.. The 510(k) number is K890986.

When did VINYL PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

VINYL PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1989-04-04, under 510(k) number K890986.

Who is the listed applicant for VINYL PATIENT EXAMINATION GLOVE?

The FDA 510(k) record lists Precious Mountain Ent. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL PATIENT EXAMINATION GLOVE?

The FDA product code for VINYL PATIENT EXAMINATION GLOVE 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 Precious Mountain Ent. Corp. 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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