INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450— 510(k) K972112

Substantially Equivalent

Taut, Inc.

FDA 510(k) clearance K972112 for INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450, Substantially Equivalent on 1997-12-01. Applicant: Taut, Inc..

Clearance details

Applicant: Taut, Inc.
Product code: Code GBW
Advisory panel: General, Plastic Surgery
Date received: 1997-06-05
Decision date: 1997-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geneva, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GBW

product code GBW

Death: 6
Total: 6

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.