TECHMEDICA MP SYSTEM— 510(k) K882922

Substantially Equivalent

Techmedica, Inc.

FDA 510(k) clearance K882922 for TECHMEDICA MP SYSTEM, Substantially Equivalent on 1988-09-22. Applicant: Techmedica, Inc..

Clearance details

Applicant: Techmedica, Inc.
Product code: Code KTT
Advisory panel: Orthopedic
Date received: 1988-07-13
Decision date: 1988-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

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Adverse events under product code KTT

product code KTT

Death: 11
Injury: 3,097
Malfunction: 1,261
Total: 4,369

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.