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

EXUSORB(TM) GEL DRESSING

K Number: K895606 · Decision Oct 19, 1989
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
4
Review Days
31

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Basic Information

Device Name
EXUSORB(TM) GEL DRESSING
K Number
K895606
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
Controlled Therapeutics Corp.
Date Received
September 18, 1989
Decision Date
October 19, 1989
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 Controlled Therapeutics Corp.

K Number Device Name
K896176 EXUSORB(TM) DRY/WET DRESSING
K894996 EXUSORB(TM) GRANULES
K894274 EXUSORB TRANSPARENT DRESSING