TENDERLIFT— 510(k) K800373

Substantially Equivalent

Competent Design

FDA 510(k) clearance K800373 for TENDERLIFT, Substantially Equivalent on 1980-03-12. Applicant: Competent Design.

Clearance details

Applicant: Competent Design
Product code: Code FMR
Advisory panel: General Hospital
Date received: 1980-02-20
Decision date: 1980-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FMR

product code FMR

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.