FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SOFTCARE BARRIER WET DRESSING

K Number: K812736 · Decision Nov 6, 1981
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
63
Review Days
38

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Basic Information

Device Name
SOFTCARE BARRIER WET DRESSING
K Number
K812736
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
The Kendal Co.
Date Received
September 29, 1981
Decision Date
November 6, 1981
Product Code
EFQ
Advisory Committee
Unknown
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
EFQ Gauze/Sponge, Internal

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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. →