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FDA 510(k)

PATIENT EXAMINATION GLOVES (LATEX)

K-Number: K892791 · 1989-08-24

ApplicantUnion Industrial Co., Ltd.
Decision Date1989-08-24
Product CodeIMM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES (LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is Union Industrial Co., Ltd.. It received FDA 510(k) clearance on 1989-08-24 under 510(k) number K892791. The device is classified under product code IMM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT EXAMINATION GLOVES (LATEX)?

PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-08-24. The listed applicant is Union Industrial Co., Ltd.. The 510(k) number is K892791.

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

PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-08-24, under 510(k) number K892791.

Who is the listed applicant for PATIENT EXAMINATION GLOVES (LATEX)?

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

What is the FDA product code for PATIENT EXAMINATION GLOVES (LATEX)?

The FDA product code for PATIENT EXAMINATION GLOVES (LATEX) is IMM.

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.

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Other records listing Union Industrial Co., 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.

K946132PROWAYK892919LATEX DISPOSABLE EXAMINATION GLOVES

Related Devices (Code: IMM)

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.

K821634EZ STAND MOBILE STOOLFred Sammons, Inc.

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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