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FDA 510(k)

TAN CHONG GLOVE, HYPOALLERGENIC

K-Number: K911146 · 1991-04-18

ApplicantBoston Medical Corp.
Decision Date1991-04-18
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAN CHONG GLOVE, HYPOALLERGENIC is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Corp.. It received FDA 510(k) clearance on 1991-04-18 under 510(k) number K911146. 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 TAN CHONG GLOVE, HYPOALLERGENIC?

TAN CHONG GLOVE, HYPOALLERGENIC is a medical device that received FDA 510(k) clearance on 1991-04-18. The listed applicant is Boston Medical Corp.. The 510(k) number is K911146.

When did TAN CHONG GLOVE, HYPOALLERGENIC receive FDA 510(k) clearance?

TAN CHONG GLOVE, HYPOALLERGENIC received FDA 510(k) clearance on 1991-04-18, under 510(k) number K911146.

Who is the listed applicant for TAN CHONG GLOVE, HYPOALLERGENIC?

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

What is the FDA product code for TAN CHONG GLOVE, HYPOALLERGENIC?

The FDA product code for TAN CHONG GLOVE, HYPOALLERGENIC is LYY.

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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.

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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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