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FDA 510(k)

DERMATOUCH LATEX GLOVES

K-Number: K955670 · 1996-03-06

ApplicantConcordia Research Lab
Decision Date1996-03-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMATOUCH LATEX GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Concordia Research Lab. It received FDA 510(k) clearance on 1996-03-06 under 510(k) number K955670. 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 DERMATOUCH LATEX GLOVES?

DERMATOUCH LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1996-03-06. The listed applicant is Concordia Research Lab. The 510(k) number is K955670.

When did DERMATOUCH LATEX GLOVES receive FDA 510(k) clearance?

DERMATOUCH LATEX GLOVES received FDA 510(k) clearance on 1996-03-06, under 510(k) number K955670.

Who is the listed applicant for DERMATOUCH LATEX GLOVES?

The FDA 510(k) record lists Concordia Research Lab as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMATOUCH LATEX GLOVES?

The FDA product code for DERMATOUCH LATEX GLOVES is LYY.

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Related Devices (Code: LYY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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