PRO-TECT TRAUMA PAK— 510(k) K941789

Substantially Equivalent

Pro-Tect Medical Products, Inc.

FDA 510(k) clearance K941789 for PRO-TECT TRAUMA PAK, Substantially Equivalent on 1995-01-12. Applicant: Pro-Tect Medical Products, Inc..

Clearance details

Applicant: Pro-Tect Medical Products, Inc.
Product code: Code MGP
Advisory panel: Unknown
Date received: 1994-04-11
Decision date: 1995-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

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.