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FDA 510(k)

PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY)

K-Number: K894090 · 1990-04-16

ApplicantEverbest Machinery (U.S.A.) Co. , Ltd.
Decision Date1990-04-16
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY) is the device name listed in this FDA 510(k) record. The listed applicant is Everbest Machinery (U.S.A.) Co. , Ltd.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K894090. 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 PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY)?

PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY) is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Everbest Machinery (U.S.A.) Co. , Ltd.. The 510(k) number is K894090.

When did PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY) receive FDA 510(k) clearance?

PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY) received FDA 510(k) clearance on 1990-04-16, under 510(k) number K894090.

Who is the listed applicant for PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY)?

The FDA 510(k) record lists Everbest Machinery (U.S.A.) Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY)?

The FDA product code for PATIENT EXAMIN GLOVES(MFG: SHANGHAI FACTORY) 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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