FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

3M TEGAGEN HI ALGINATE DRESSING & 3M TEGAGEN HG ALGINATE DRESSING

K Number: K980989 · Decision May 27, 1998
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
14
Review Days
72

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Basic Information

Device Name
3M TEGAGEN HI ALGINATE DRESSING & 3M TEGAGEN HG ALGINATE DRESSING
K Number
K980989
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovative Technologies , Ltd.
Date Received
March 16, 1998
Decision Date
May 27, 1998
Product Code
KMF
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KMF Bandage, Liquid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KMF), ordered by most recent decision date.

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Other Clearances by Innovative Technologies , Ltd.

K Number Device Name
K983303 INNOVATIVE TECHNOLOGIES HYDROCOLLOID AND INTELLIGENT HYDROCOLLOID WOUND DRESSINGS
K982234 AL-GEN CALCIUM ALGINATE DRESSING
K982638 3M TEGAGEN HI ALGINATE DRESSING & 3 M TEGAGEN HG ALGINATE DRESSING, MODEL #'S 90110,90112,90114,90120, 90210,90212,90214
K981753 INNOVATIVE TECHNOLOGIES TRANSPARENT FILM AND INTELLIGENT FILM WOUND DRESSING
K980097 FLEXIGEL-G HYDROGEL WOUND DRESSING
K973855 IT HYDROCOLLOID WITH ZINC
K973312 TRANSPARENT FILM DRESSING, INTELLIGENT FILM DRESSING
K973283 ALGINATE/ZINC WOUND DRESSING
K971126 HYDROCOLLOID WOUND DRESSINGS
K963598 INNOVATIVE TECHNOLOGIES ALIGINATE/PECTIN WOUND DRESSINGS
Search all 14 clearances from Innovative Technologies , Ltd. →