GELFLEX— 510(k) K940848

Substantially Equivalent

Venture Management Corp.

FDA 510(k) clearance K940848 for GELFLEX, Substantially Equivalent on 1995-04-07. Applicant: Venture Management Corp..

Clearance details

Applicant: Venture Management Corp.
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 1994-02-23
Decision date: 1995-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brooklyn, CT, US

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Adverse events under product code LPL

product code LPL

Injury: 988
Other: 4
Total: 992

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.