Capd U.V. Germicidal Connection System

FDA 510(k) K812802 · Travenol Laboratories, S.A.

Substantially Equivalent

510(k) numberK812802

Submission

Device name
Capd U.V. Germicidal Connection System
Applicant
Travenol Laboratories, S.A.
Walker, MI, US
Received
October 6, 1981
Decision date
March 2, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KDJ – Set, Administration, For Peritoneal Dialysis, Disposable
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5630
Specialty
Gastroenterology, Urology
Life-sustaining
Yes

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More from Baxter Healthcare Corporation

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K874181Baxter Bedside SystemFRN · Traditional 02/22/1988SE
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K873873Resubmitted Micron Transfusion FilterCAK · Traditional 10/22/1987SE
K873984Automatic Peritoneal Dialysis Cycler Set (5C4437)KDJ · Traditional 10/20/1987SE
K872364Hemodialysis (SPS), Model 550, Code 5M1309FII · Traditional 10/13/1987SE
K872652Upgraded Auto Peritoneal Dialysis Cycler SystemFKX · Traditional 09/30/1987SE
K870801Flo-Gard 6200 Volumetric Infusion/Pumping BloodFRN · Traditional 09/04/1987SE
K871908IV Administration SetBRZ · Traditional 07/27/1987SE
K871471Capillary Flow Dialyzers Models ST-12 & ST-15FJI · Traditional 06/12/1987SE
K865029Continu-Flo Solution Admin. Set W/In-Line FilterFPB · Traditional 04/17/1987SE

Questions and answers

When was Capd U.V. Germicidal Connection System cleared by the FDA?

Capd U.V. Germicidal Connection System (K812802) received a 510(k) decision of Substantially Equivalent on March 2, 1982, 147 days after the submission was received.

What is the product code of K812802?

The FDA product code is KDJ – Set, Administration, For Peritoneal Dialysis, Disposable, a Class II (moderate risk) device regulated under 21 CFR 876.5630.