Solcotrans Orthopaedic Drainage/Reinfusion System

FDA 510(k) K913247 · Solco Basle, Inc.

Substantially Equivalent

510(k) numberK913247

Submission

Device name
Solcotrans Orthopaedic Drainage/Reinfusion System
Applicant
Solco Basle, Inc.
Hingham, MA, US
Received
July 22, 1991
Decision date
February 25, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CAC – Apparatus, Autotransfusion
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5830
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Fresenius Kabi AG

510(k)DeviceDecision
K913177Solcotrans Orthopaedic Drainage/Reinfusion SystemCAC · Traditional 02/25/1993SE
K915867Solcovac Wound Drainage SystemGCY · Traditional 08/14/1992SESK
K896858Solcotrans Intraoperative Autotransfusion SystemCAC · Traditional 04/05/1990SE
K896857Solcotrans Orthopaedic Drainage/Reinfusion SystemCAC · Traditional 04/05/1990SE
K896203Solcosept(Tm) Blood Transfusion FilterCAK · Traditional 02/01/1990SE
K883058Solcotrans Ortho. Drainage/Reinfusion SystemCAC · Traditional 10/28/1988SE
K872590Solcotrans Chest Drainage Autotransfusion SystemCAC · Traditional 09/04/1987SE
K872157Hall Vein StripperDWQ · Traditional 07/07/1987SE
K843821Solco Basle Intraoperative AutottrnsfusCAC · Traditional 10/01/1985SE

Questions and answers

When was Solcotrans Orthopaedic Drainage/Reinfusion System cleared by the FDA?

Solcotrans Orthopaedic Drainage/Reinfusion System (K913247) received a 510(k) decision of Substantially Equivalent on February 25, 1993, 584 days after the submission was received.

What is the product code of K913247?

The FDA product code is CAC – Apparatus, Autotransfusion, a Class II (moderate risk) device regulated under 21 CFR 868.5830.