FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

FOLEY INSERTION TRAY

K Number: K923906 · Decision Jun 22, 1993
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
13
Review Days
322

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Basic Information

Device Name
FOLEY INSERTION TRAY
K Number
K923906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Kit Pak, Inc.
Date Received
August 4, 1992
Decision Date
June 22, 1993
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 Kit Pak, Inc.

K Number Device Name
K942959 KIT PAK WET SALINE DRESSING
K941499 KIT PAK DRESSING CHANGE TRAY
K932310 KIT PAK INCONTINENT SKIN CARE KIT
K934080 URINARY DRAINAGE BAG
K931013 FOLEY CATHETER TRAY
K923905 WOUND DRESSING KIT
K924051 KIT PAK I.V. START KIT
K922051 KIT PAK'S FLUSHING KIT
K925281 KIT PAK URINARY CARE SUPPLIES
K900148 KIT PAK IRRIGATION TRAY
Search all 13 clearances from Kit Pak, Inc. →