Conphar Urinary Drainage BAG-2000ML

FDA 510(k) K791265 · Conphar, Inc.

Substantially Equivalent

510(k) numberK791265

Submission

Device name
Conphar Urinary Drainage BAG-2000ML
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
July 6, 1979
Decision date
September 7, 1979
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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Questions and answers

When was Conphar Urinary Drainage BAG-2000ML cleared by the FDA?

Conphar Urinary Drainage BAG-2000ML (K791265) received a 510(k) decision of Substantially Equivalent on September 7, 1979, 63 days after the submission was received.

What is the product code of K791265?

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.