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FDA 510(k)

PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL)

K-Number: K891942 · 1989-05-08

ApplicantLc Saratoga International, Inc.
Decision Date1989-05-08
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL) is the device name listed in this FDA 510(k) record. The listed applicant is Lc Saratoga International, Inc.. It received FDA 510(k) clearance on 1989-05-08 under 510(k) number K891942. 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. JENQ CHUAM INDUSTRIAL)?

PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL) is a medical device that received FDA 510(k) clearance on 1989-05-08. The listed applicant is Lc Saratoga International, Inc.. The 510(k) number is K891942.

When did PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL) received FDA 510(k) clearance on 1989-05-08, under 510(k) number K891942.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL)?

The FDA 510(k) record lists Lc Saratoga International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL)?

The FDA product code for PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL) is LYY.

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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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