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FDA 510(k)

PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL

K-Number: K893696 · 1989-09-29

ApplicantDouble Scores , Ltd.
Decision Date1989-09-29
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL is the device name listed in this FDA 510(k) record. The listed applicant is Double Scores , Ltd.. It received FDA 510(k) clearance on 1989-09-29 under 510(k) number K893696. 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 EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL?

PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL is a medical device that received FDA 510(k) clearance on 1989-09-29. The listed applicant is Double Scores , Ltd.. The 510(k) number is K893696.

When did PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL receive FDA 510(k) clearance?

PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL received FDA 510(k) clearance on 1989-09-29, under 510(k) number K893696.

Who is the listed applicant for PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL?

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

What is the FDA product code for PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL?

The FDA product code for PATIENT EXAM GLOVES(MFG: JIN DING ZAI JIE LATEX GL is LYY.

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Official Source

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