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510(k) K944379

ORION'S FOLEY CATHETERIZATION KIT WITH CATHETER AND BAG by Regulatory & Marketing Services, Inc. — Product Code FGM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 15, 1995
Date Received
September 7, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Probe And Director, Gastro-Urology
Device Class
Class I
Regulation Number
876.4730
Review Panel
GU
Submission Type

Other clearances by Regulatory & Marketing Services, Inc.

  • K101721 — WELL LEAD TRACHEOSTOMY TUBE AND DISPOSABLE INNER CANNULA (March 24, 2011)
  • K944673 — MRI'S ALL SILICONE FOLEY CATHETER TEMPERATURE PROBE (April 10, 1996)
  • K954752 — PEDIATRIC EUROPHYLIC FOLEY CATHETER (October 30, 1995)
  • K941342 — PAIN DOC (October 13, 1995)
  • K941543 — DIAL MEDICAL KIT (February 16, 1995)
  • K944384 — ORION'S URETHRAL CATHETERIZATION KIT WITHOUT BAG (February 15, 1995)
  • K944378 — ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG (February 15, 1995)
  • K945874 — EUROMEDICAL POLY TRACHEOTOMY TUBE (December 27, 1994)
  • K944383 — ORION RED URETHRAL CATHETER (December 6, 1994)
  • K944377 — ORION'S URINARY DRAINAGE SET (December 6, 1994)

Other clearances for product code FGM

  • K041732 — CAVERMAP SURGICAL AID (September 21, 2004)
  • K031527 — MODIFICATION TO CAVERMAP SURGICAL AID (June 5, 2003)
  • K010098 — MODIFICATION TO CAVERMAP SURGICAL AID (February 1, 2001)
  • K993436 — CAVERMAP SURGICAL AID (February 11, 2000)
  • K944384 — ORION'S URETHRAL CATHETERIZATION KIT WITHOUT BAG (February 15, 1995)
  • K944378 — ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG (February 15, 1995)