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

TRACHEOSTOMY CARE TRAY

K Number: K923156 · Decision Aug 18, 1993
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
33
Review Days
415

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Basic Information

Device Name
TRACHEOSTOMY CARE TRAY
K Number
K923156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent for Some Indications
Applicant
Orion Life Systems, Inc.
Date Received
June 29, 1992
Decision Date
August 18, 1993
Product Code
JOH
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
JOH Tube Tracheostomy And Tube Cuff

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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. →