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

CLINIGUARD STERILE

K Number: K810240 · Decision Feb 19, 1981
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
221
Applicant Total
16
Review Days
22

Basic Information

Device Name
CLINIGUARD STERILE
K Number
K810240
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
CLINIPAD CORP.
Date Received
January 28, 1981
Decision Date
February 19, 1981
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

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Other Clearances by CLINIPAD CORP.

K Number Device Name
K931560 CARDIAC CATHETERIZATION TRAY
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K932071 I.V. START KIT
K932010 V.A.D. ACCESS KIT
K932036 LACERATION TRAY
K932016 TRACHEOSTOMY CARE TRAY
K862562 PUNCH BIOPSY KIT
K862563 TRACHEOSTOMY CLEANSING SOLUTION
K833075 WET DRESSING KIT
K833432 CATHETER INSERTION KIT
Search all 16 clearances from CLINIPAD CORP. →