MYO-ACTUATOR— 510(k) K852963

Substantially Equivalent

Verimed Holdings, Inc.

FDA 510(k) clearance K852963 for MYO-ACTUATOR, Substantially Equivalent on 1986-01-21. Applicant: Verimed Holdings, Inc.. Device class: 2.

Clearance details

Applicant: Verimed Holdings, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1985-07-12
Decision date: 1986-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Verimed Holdings, Inc.

K981277 — PERIFORM1998-11-20
K954127 — BIOFEEDBACK DEVICE1995-11-14
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K930670 — PHYACTION 7871993-07-02
K922550 — ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)1992-12-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.