DAVIS+GECK VISADUCT KIT— 510(k) K894685

Substantially Equivalent

Davis & Geck, Inc.

FDA 510(k) clearance K894685 for DAVIS+GECK VISADUCT KIT, Substantially Equivalent on 1989-08-22. Applicant: Davis & Geck, Inc..

Clearance details

Applicant: Davis & Geck, Inc.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1989-07-25
Decision date: 1989-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danbury, CT, US

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Adverse events under product code LRO

product code LRO

Injury: 975
Malfunction: 14,038
Other: 2
Total: 15,015

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.