SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM— 510(k) K913247

Name: FDA 510(k) clearance K913247
Creator: U.S. Food and Drug Administration
Published: 1993-02-25

Substantially Equivalent

Solco Basle, Inc.

FDA 510(k) clearance K913247 for SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM, Substantially Equivalent on 1993-02-25. Applicant: Solco Basle, Inc.. Device class: 2.

Clearance details

Applicant: Solco Basle, Inc.
Product code: Code CAC
Device class: Class 2
Regulation: 21 CFR 868.5830
Advisory panel: Anesthesiology
Date received: 1991-07-22
Decision date: 1993-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hingham, MA, US

Download summary PDF View on FDA.gov ↗

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K913177 — SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM1993-02-25
K915867 — SOLCOVAC WOUND DRAINAGE SYSTEM1992-08-14
K896857 — SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM1990-04-05
K896858 — SOLCOTRANS INTRAOPERATIVE AUTOTRANSFUSION SYSTEM1990-04-05
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Adverse events under product code CAC

product code CAC

Death: 11
Malfunction: 477
Total: 488

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.