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

ORION CENTRAL LINE DRESSING CHANGE TRAY

K Number: K941542 · Decision May 23, 1994
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
21
Review Days
54

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Basic Information

Device Name
ORION CENTRAL LINE DRESSING CHANGE TRAY
K Number
K941542
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Regulatory & Marketing Services, Inc.
Date Received
March 30, 1994
Decision Date
May 23, 1994
Product Code
FRG
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
FRG Wrap, Sterilization

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K941342 PAIN DOC
K941543 DIAL MEDICAL KIT
K944378 ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG
K944384 ORION'S URETHRAL CATHETERIZATION KIT WITHOUT BAG
K944379 ORION'S FOLEY CATHETERIZATION KIT WITH CATHETER AND BAG
K945874 EUROMEDICAL POLY TRACHEOTOMY TUBE
K944383 ORION RED URETHRAL CATHETER
K944382 ORION ALL SILICONE FOLEY CATHETER
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