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FDA 510(k)

VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.)

K-Number: K892318 · 1989-08-22

Decision Date1989-08-22
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.) is the device name listed in this FDA 510(k) record. The listed applicant is Svenska Medita Ac.. It received FDA 510(k) clearance on 1989-08-22 under 510(k) number K892318. 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 EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.)?

VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.) is a medical device that received FDA 510(k) clearance on 1989-08-22. The listed applicant is Svenska Medita Ac.. The 510(k) number is K892318.

When did VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.) receive FDA 510(k) clearance?

VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.) received FDA 510(k) clearance on 1989-08-22, under 510(k) number K892318.

Who is the listed applicant for VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.)?

The FDA 510(k) record lists Svenska Medita Ac. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.)?

The FDA product code for VINYL EXAM GLOVES (MFG. UNIVERSAL GLOVE CORP.) 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 Svenska Medita Ac. 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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