TISSUEBAG, MODELS: A10 211, A10 212, TBI 100, TBI1011, TBI1021— 510(k) K092821

Substantially Equivalent

Agency For Medical Innovations, Inc.

FDA 510(k) clearance K092821 for TISSUEBAG, MODELS: A10 211, A10 212, TBI 100, TBI1011, TBI1021, Substantially Equivalent on 2010-02-01. Applicant: Agency For Medical Innovations, Inc..

Clearance details

Applicant: Agency For Medical Innovations, Inc.
Product code: Code GCJ
Advisory panel: Gastroenterology, Urology
Date received: 2009-09-14
Decision date: 2010-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Natick, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GCJ

product code GCJ

Death: 39
Injury: 1,638
Malfunction: 28,216
Other: 11
Total: 29,904

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.