SCALAMOBIL— 510(k) K920105

Substantially Equivalent

Alber Technologies, Inc.

FDA 510(k) clearance K920105 for SCALAMOBIL, Substantially Equivalent on 1992-08-06. Applicant: Alber Technologies, Inc..

Clearance details

Applicant: Alber Technologies, Inc.
Product code: Code ING
Advisory panel: Physical Medicine
Date received: 1992-01-09
Decision date: 1992-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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Adverse events under product code ING

product code ING

Death: 3
Total: 3

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.