CONMED VENI-GARD(TM I.V. DRESSING-PRODUCT LINE EXTENSION AND MODIFICATIONS— 510(k) K950065

Name: FDA 510(k) clearance K950065
Creator: U.S. Food and Drug Administration
Published: 1995-03-24

Substantially Equivalent

Conmedcorp

FDA 510(k) clearance K950065 for CONMED VENI-GARD(TM I.V. DRESSING-PRODUCT LINE EXTENSION AND MODIFICATIONS, Substantially Equivalent on 1995-03-24. Applicant: Conmedcorp. Device class: Unclassified.

Clearance details

Applicant: Conmedcorp
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-01-09
Decision date: 1995-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dayton, OH, US

Download summary PDF View on FDA.gov ↗

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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.