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FDA 510(k)

EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX)

K-Number: K891667 · 1989-08-25

ApplicantSan HU Chemical Industry Co., Ltd.
Decision Date1989-08-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is San HU Chemical Industry Co., Ltd.. It received FDA 510(k) clearance on 1989-08-25 under 510(k) number K891667. 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 EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX)?

EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX) is a medical device that received FDA 510(k) clearance on 1989-08-25. The listed applicant is San HU Chemical Industry Co., Ltd.. The 510(k) number is K891667.

When did EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX) receive FDA 510(k) clearance?

EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX) received FDA 510(k) clearance on 1989-08-25, under 510(k) number K891667.

Who is the listed applicant for EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX)?

The FDA 510(k) record lists San HU Chemical Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX)?

The FDA product code for EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX) is LYY.

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Official Source

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