RECOVER ADULT VEIN WARMER— 510(k) K963689

Substantially Equivalent

Florida Medical Industries, Inc.

FDA 510(k) clearance K963689 for RECOVER ADULT VEIN WARMER, Substantially Equivalent on 1996-12-12. Applicant: Florida Medical Industries, Inc..

Clearance details

Applicant: Florida Medical Industries, Inc.
Product code: Code IMD
Advisory panel: Physical Medicine
Date received: 1996-09-16
Decision date: 1996-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarpon Springs, FL, US

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Adverse events under product code IMD

product code IMD

Death: 3
Injury: 600
Total: 603

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.