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

CATHETER INSERTION KIT

K Number: K833432 · Decision Dec 28, 1983
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
16
Review Days
84

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Basic Information

Device Name
CATHETER INSERTION KIT
K Number
K833432
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Clinipad Corp.
Date Received
October 5, 1983
Decision Date
December 28, 1983
Product Code
KOD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KOD Catheter, Urological

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Other Clearances by Clinipad Corp.

K Number Device Name
K931560 CARDIAC CATHETERIZATION TRAY
K931668 PICC INSERTION TRAY
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
K830476 OR PREP KIT
Search all 16 clearances from Clinipad Corp. →