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

URINARY CARE SUPPLIES

K Number: K923496 · Decision May 27, 1993
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
33
Review Days
316

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Basic Information

Device Name
URINARY CARE SUPPLIES
K Number
K923496
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Orion Life Systems, Inc.
Date Received
July 15, 1992
Decision Date
May 27, 1993
Product Code
KNY
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
KNY Accessories, Catheter, G-U

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNY), ordered by most recent decision date.

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Other Clearances by Orion Life Systems, Inc.

K Number Device Name
K943835 PRE-FILLED SYRINGE W/STERILE .25% ACETC ACID
K943834 STERILE .9% SODIUM CHLORIDE SOLUTION
K943830 PRE-FILLED SYRINGE W/STERILE 0.9% SODIUM CHLORIDE SOLUTION
K943836 PRE-FILLED 10CC INFLATION SYRINGE W/STERILE WATER
K943831 PRE-FILLED 30CC INFLATION SYRINGE W/STERILE WATER
K943832 STERILE .9% SODIUM CHLORIDE FOR IRRATION
K943829 PRE-FILLED SYSRINGE W/STERILE WATER
K943828 STERILE WATER FOR IRRIGATION
K943833 STERILE WATER FOR IRRATION
K923168 DUAL PORT ENTERAL Y-ADAPTOR
Search all 33 clearances from Orion Life Systems, Inc. →