MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I— 510(k) K992694

Substantially Equivalent

Myotronics-Noromed, Inc.

FDA 510(k) clearance K992694 for MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I, Substantially Equivalent on 1999-09-10. Applicant: Myotronics-Noromed, Inc..

Clearance details

Applicant: Myotronics-Noromed, Inc.
Product code: Code KZM
Advisory panel: Physical Medicine
Date received: 1999-08-12
Decision date: 1999-09-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Tukwila, WA, US

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