CELL SAVER HAEMOLITE B AUTO. BLOOD RECOVERY SYSTEM— 510(k) K883934

Name: FDA 510(k) clearance K883934
Creator: U.S. Food and Drug Administration
Published: 1988-12-27

Substantially Equivalent

Haemonetics Corp.

FDA 510(k) clearance K883934 for CELL SAVER HAEMOLITE B AUTO. BLOOD RECOVERY SYSTEM, Substantially Equivalent on 1988-12-27. Applicant: Haemonetics Corp.. Device class: 2.

Clearance details

Applicant: Haemonetics Corp.
Product code: Code CAC
Device class: Class 2
Regulation: 21 CFR 868.5830
Advisory panel: Anesthesiology
Date received: 1988-09-15
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Braintree, MA, US

Download summary PDF View on FDA.gov ↗

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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.