FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUBCLAVIAN INSERTION KIT

K Number: K820171 · Decision Mar 2, 1982
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
16
Review Days
40

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Basic Information

Device Name
SUBCLAVIAN INSERTION KIT
K Number
K820171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Clinipad Corp.
Date Received
January 21, 1982
Decision Date
March 2, 1982
Product Code
FRG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FRG Wrap, Sterilization

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Other Clearances by Clinipad Corp.

K Number Device Name
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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. →