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FDA 510(k)

EPVC PATIENT EXAMINATION GLOVE

K-Number: K896938 · 1990-03-27

ApplicantUnited Orient, Inc.
Decision Date1990-03-27
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EPVC PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is United Orient, Inc.. It received FDA 510(k) clearance on 1990-03-27 under 510(k) number K896938. 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 EPVC PATIENT EXAMINATION GLOVE?

EPVC PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1990-03-27. The listed applicant is United Orient, Inc.. The 510(k) number is K896938.

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

EPVC PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1990-03-27, under 510(k) number K896938.

Who is the listed applicant for EPVC PATIENT EXAMINATION GLOVE?

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

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

The FDA product code for EPVC PATIENT EXAMINATION GLOVE is LYZ.

Related Clinical Trials

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Other records listing United Orient, 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.

K901213LATEX EXAMINATION GLOVES

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.

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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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