FDA 510(k) FDA unclassified Unknown 🇺🇸 United States

WOUND TREATMENT KIT

K Number: K901109 · Decision Jun 6, 1990
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
33
Review Days
89

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Basic Information

Device Name
WOUND TREATMENT KIT
K Number
K901109
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Unknown
Applicant
Orion Life Systems, Inc.
Date Received
March 9, 1990
Decision Date
June 6, 1990
Product Code
FRO
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FRO Dressing, Wound, Drug

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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. →