FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

KIT PAK I.V. START KIT

K Number: K924051 · Decision Jun 22, 1993
Classifications
1
FEI Numbers
169
Registration Numbers
169
Same Product Code
1953
Applicant Total
13
Review Days
314

Basic Information

Device Name
KIT PAK I.V. START KIT
K Number
K924051
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
KIT PAK, INC.
Date Received
August 12, 1992
Decision Date
June 22, 1993
Product Code
LYY
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
LYY Latex Patient Examination Glove

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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
K923906 FOLEY INSERTION TRAY
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. →