FDA 510(k)

STERILE WET DRESSING PACK

K-Number: K810406 · 1981-03-11

Decision Date1981-03-11

Product Code

DecisionSubstantially Equivalent

Device Summary

STERILE WET DRESSING PACK is the device name listed in this FDA 510(k) record. The listed applicant is W.G. Whitney Corp.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810406. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE WET DRESSING PACK?

STERILE WET DRESSING PACK is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is W.G. Whitney Corp.. The 510(k) number is K810406.

When did STERILE WET DRESSING PACK receive FDA 510(k) clearance?

STERILE WET DRESSING PACK received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810406.

Who is the listed applicant for STERILE WET DRESSING PACK?

The FDA 510(k) record lists W.G. Whitney Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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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Other records listing W.G. Whitney Corp. as applicant

K834532STERILE WET DRESSING PACK K813535XEROFORM DRESSING K803299COLD/HOT PACK K800907TOMAC WET DRESSING WARMER K781322STERILE WET DRESSING PACK K770387UNICATCH

View all 7 devices →

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.