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

CONFORMA(TM) PLASTER BANDAGES

K Number: K873111 · Decision Oct 9, 1987
Classifications
1
FEI Numbers
238
Registration Numbers
238
Same Product Code
36
Applicant Total
63
Review Days
60

Basic Information

Device Name
CONFORMA(TM) PLASTER BANDAGES
K Number
K873111
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
THE KENDAL CO.
Date Received
August 10, 1987
Decision Date
October 9, 1987
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 THE KENDAL CO.

K Number Device Name
K000087 MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
K990500 KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C
K991758 MONOJECT INSULIN SYRINGE
K970969 KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
K951488 KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
K942664 KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
K942774 POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING
K892434 KENDALL CURITY OXYGEN MASK
K892438 KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
K892440 KENDALL CURITY EXTENSION TUBES
Search all 63 clearances from THE KENDAL CO. →