FDA 510(k)

ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE

K-Number: K891791 · 1989-07-14

Decision Date1989-07-14

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K891791. 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 ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE?

ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Medline Industries, Inc.. The 510(k) number is K891791.

When did ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE receive FDA 510(k) clearance?

ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE received FDA 510(k) clearance on 1989-07-14, under 510(k) number K891791.

Who is the listed applicant for ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE?

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

What is the FDA product code for ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE?

The FDA product code for ACCU-TOUCH LATEX EXAM GLOVES, UNISIZE & LARGE 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.