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FDA 510(k)

CLEAN HAND-VCL GLOVE DISPENSER

K-Number: K897048 · 1990-01-25

Decision Date1990-01-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLEAN HAND-VCL GLOVE DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Safety Today, Inc.. It received FDA 510(k) clearance on 1990-01-25 under 510(k) number K897048. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAN HAND-VCL GLOVE DISPENSER?

CLEAN HAND-VCL GLOVE DISPENSER is a medical device that received FDA 510(k) clearance on 1990-01-25. The listed applicant is Safety Today, Inc.. The 510(k) number is K897048.

When did CLEAN HAND-VCL GLOVE DISPENSER receive FDA 510(k) clearance?

CLEAN HAND-VCL GLOVE DISPENSER received FDA 510(k) clearance on 1990-01-25, under 510(k) number K897048.

Who is the listed applicant for CLEAN HAND-VCL GLOVE DISPENSER?

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

What is the FDA product code for CLEAN HAND-VCL GLOVE DISPENSER?

The FDA product code for CLEAN HAND-VCL GLOVE DISPENSER is LYY.

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.

Related Devices (Code: LYY)

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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