MM-1 MOVEMENT MONITOR— 510(k) K971318

Substantially Equivalent

Axon Instruments, Inc.

FDA 510(k) clearance K971318 for MM-1 MOVEMENT MONITOR, Substantially Equivalent on 1997-07-28. Applicant: Axon Instruments, Inc..

Clearance details

Applicant: Axon Instruments, Inc.
Product code: Code GYD
Advisory panel: Neurology
Date received: 1997-04-09
Decision date: 1997-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

Download summary PDF View on FDA.gov ↗

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