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

CELLAMIN

K Number: K802796 · Decision Nov 24, 1980
Classifications
1
FEI Numbers
239
Registration Numbers
239
Same Product Code
36
Applicant Total
18
Review Days
20

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CELLAMIN
K Number
K802796
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Secol Co.
Date Received
November 4, 1980
Decision Date
November 24, 1980
Product Code
ITG
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ITG Bandage, Cast

Similar 510(k) Clearances

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

View all

Other Clearances by Secol Co.

K Number Device Name
K802790 SOLVALINE
K810111 CELLONA PLASTER VARNISH
K810109 METAL SPLINTS
K810110 COBBLER'S CHIP SPLINTS
K802794 PRO-OPHTA STICKS
K802793 LOMATUELL OINTMENT DRESSING
K802799 EYE PADS
K802797 O.R. DRAPES
K802791 ZINC PASTE BANDAGE
K802787 METALLINE DRESSINGS
Search all 18 clearances from Secol Co. →