Foam Calcium Aliginate Topical Wound Dressing

FDA 510(k) K963656 · Adri

Substantially Equivalent

510(k) numberK963656

Submission

Device name
Foam Calcium Aliginate Topical Wound Dressing
Applicant
Adri
Park Forest, IL, US
Received
September 12, 1996
Decision date
November 12, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KMF – Bandage, Liquid
Device class
Class I (low risk)
Regulation
21 CFR 880.5090
Specialty
General Hospital

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More from Polichem S.A

510(k)DeviceDecision
K041268Silversite or CalgitrolMGQ · Traditional 09/20/2004SE
K011618Calgitrol AG Silver Alginate Wound DressingFRO · Traditional 11/15/2002SE
K000054Foam Calcium Alginate Topical Wound Dressing with CollagenKGN · Traditional 03/13/2000SE
K940404Alginate Fiber Topical Wound DressingKMF · Traditional 05/04/1994SN
K870383Alginate Wool FiberKHR · Traditional 04/30/1987SE

Questions and answers

When was Foam Calcium Aliginate Topical Wound Dressing cleared by the FDA?

Foam Calcium Aliginate Topical Wound Dressing (K963656) received a 510(k) decision of Substantially Equivalent on November 12, 1996, 61 days after the submission was received.

What is the product code of K963656?

The FDA product code is KMF – Bandage, Liquid, a Class I (low risk) device regulated under 21 CFR 880.5090.