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FDA 510(k)

MEDI, CURI EXAM GLOVES

K-Number: K893060 · 1990-09-04

ApplicantGolden Charter , Ltd.
Decision Date1990-09-04
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI, CURI EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Golden Charter , Ltd.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K893060. 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 MEDI, CURI EXAM GLOVES?

MEDI, CURI EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Golden Charter , Ltd.. The 510(k) number is K893060.

When did MEDI, CURI EXAM GLOVES receive FDA 510(k) clearance?

MEDI, CURI EXAM GLOVES received FDA 510(k) clearance on 1990-09-04, under 510(k) number K893060.

Who is the listed applicant for MEDI, CURI EXAM GLOVES?

The FDA 510(k) record lists Golden Charter , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI, CURI EXAM GLOVES?

The FDA product code for MEDI, CURI EXAM GLOVES is LYY.

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Official Source

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