Bag, Urine Collection, Closed System

FDA 510(k) K760105 · Concord Laboratories, Inc.

Substantially Equivalent

510(k) numberK760105

Submission

Device name
Bag, Urine Collection, Closed System
Applicant
Concord Laboratories, Inc.
Mchenry, IL, US
Received
June 24, 1976
Decision date
October 7, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNX – Collector, Urine, (And Accessories) For Indwelling Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5250
Specialty
Gastroenterology, Urology

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More from Bristol-Myers Squibb

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K864535Tracheobronchial Suction Catheter, Cat. No. 6110BSY · Traditional 01/06/1987SE
K862039Concord Care Tray · Traditional 07/03/1986SESD
K854601Spring Guide Catheter Anesthesia Conduction CathBSO · Traditional 01/10/1986SE
K854327Subcutaneous Tunneling Needles & HandlesGCB · Traditional 11/13/1985SE
K851134Regional Anesthesia TraysCAZ · Traditional 07/15/1985SESD
K842095Epidural TraysCAZ · Traditional 07/03/1984SE
K841486Arterial Blood Sampling KitsCBT · Traditional 05/23/1984SE
K840987Vaporized HeparinCBT · Traditional 04/05/1984SE

Questions and answers

When was Bag, Urine Collection, Closed System cleared by the FDA?

Bag, Urine Collection, Closed System (K760105) received a 510(k) decision of Substantially Equivalent on October 7, 1976, 105 days after the submission was received.

What is the product code of K760105?

The FDA product code is KNX – Collector, Urine, (And Accessories) For Indwelling Catheter, a Class II (moderate risk) device regulated under 21 CFR 876.5250.