FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG

K Number: K944378 · Decision Feb 15, 1995
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
6
Applicant Total
21
Review Days
161

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG
K Number
K944378
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Regulatory & Marketing Services, Inc.
Date Received
September 7, 1994
Decision Date
February 15, 1995
Product Code
FGM
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
FGM Probe And Director, Gastro-Urology

Similar 510(k) Clearances

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

View all

Other Clearances by Regulatory & Marketing Services, Inc.

K Number Device Name
K944673 MRI'S ALL SILICONE FOLEY CATHETER TEMPERATURE PROBE
K954752 PEDIATRIC EUROPHYLIC FOLEY CATHETER
K941342 PAIN DOC
K941543 DIAL MEDICAL KIT
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
K944377 ORION'S URINARY DRAINAGE SET
Search all 21 clearances from Regulatory & Marketing Services, Inc. →