PRO-TECT SAFETY DRESSING— 510(k) K941790

Name: FDA 510(k) clearance K941790
Creator: U.S. Food and Drug Administration
Published: 1995-01-12

Substantially Equivalent

Pro-Tect Medical Products, Inc.

FDA 510(k) clearance K941790 for PRO-TECT SAFETY DRESSING, Substantially Equivalent on 1995-01-12. Applicant: Pro-Tect Medical Products, Inc.. Device class: Unclassified.

Clearance details

Applicant: Pro-Tect Medical Products, Inc.
Product code: Code MGP
Device class: Unclassified
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 ↗

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K941789 — PRO-TECT TRAUMA PAK1995-01-12

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.