MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000— 510(k) K030332

Substantially Equivalent

Bionicare Medical Technologies, Inc.

FDA 510(k) clearance K030332 for MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000, Substantially Equivalent on 2003-06-06. Applicant: Bionicare Medical Technologies, Inc..

Clearance details

Applicant: Bionicare Medical Technologies, Inc.
Product code: Code NYN
Advisory panel: Neurology
Date received: 2003-01-31
Decision date: 2003-06-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Sparks, MD, US

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