MINICLINIC TM— 510(k) K771922

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K771922 for MINICLINIC TM, Substantially Equivalent on 1977-11-02. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code DTC
Advisory panel: Cardiovascular
Date received: 1977-10-13
Decision date: 1977-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DTC

product code DTC

Injury: 136
Malfunction: 3,400
Total: 3,536

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.