Solco Basle Intraoperative Autottrnsfus

FDA 510(k) K843821 · Solco Basle, Inc.

Substantially Equivalent

510(k) numberK843821

Submission

Device name
Solco Basle Intraoperative Autottrnsfus
Applicant
Solco Basle, Inc.
Walker, MI, US
Received
September 28, 1984
Decision date
October 1, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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

Questions and answers

When was Solco Basle Intraoperative Autottrnsfus cleared by the FDA?

Solco Basle Intraoperative Autottrnsfus (K843821) received a 510(k) decision of Substantially Equivalent on October 1, 1985, 368 days after the submission was received.

What is the product code of K843821?

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