FINGER MUSCLE TESTER— 510(k) K770164

Name: FDA 510(k) clearance K770164
Creator: U.S. Food and Drug Administration
Published: 1977-01-28

Substantially Equivalent

Bel-Art Products

FDA 510(k) clearance K770164 for FINGER MUSCLE TESTER, Substantially Equivalent on 1977-01-28. Applicant: Bel-Art Products. Device class: 2.

Clearance details

Applicant: Bel-Art Products
Product code: Code ISD
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 1977-01-25
Decision date: 1977-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ISD

product code ISD

Other: 2
Total: 2

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.