ProCell Surgical Sponge-Blood Recovery Unit— 510(k) K193361

Name: FDA 510(k) clearance K193361
Creator: U.S. Food and Drug Administration
Published: 2020-06-01

Substantially Equivalent

Procell Surgical, Inc.

FDA 510(k) clearance K193361 for ProCell Surgical Sponge-Blood Recovery Unit, Substantially Equivalent on 2020-06-01. Applicant: Procell Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Procell Surgical, Inc.
Product code: Code CAC
Device class: Class 2
Regulation: 21 CFR 868.5830
Advisory panel: Anesthesiology
Date received: 2019-12-04
Decision date: 2020-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, CA

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.