FDA 510(k)

HERMAL WOUND CARE KIT

K-Number: K895817 · 1990-01-19

ApplicantStiefel Research Institute, Inc.

Decision Date1990-01-19

Product CodeNAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

HERMAL WOUND CARE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Stiefel Research Institute, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K895817. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERMAL WOUND CARE KIT?

HERMAL WOUND CARE KIT is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Stiefel Research Institute, Inc.. The 510(k) number is K895817.

When did HERMAL WOUND CARE KIT receive FDA 510(k) clearance?

HERMAL WOUND CARE KIT received FDA 510(k) clearance on 1990-01-19, under 510(k) number K895817.

Who is the listed applicant for HERMAL WOUND CARE KIT?

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

What is the FDA product code for HERMAL WOUND CARE KIT?

The FDA product code for HERMAL WOUND CARE KIT is NAD.

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Other records listing Stiefel Research Institute, Inc. as applicant

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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.