PROSTIM 1000/2000— 510(k) K073438

Substantially Equivalent

Bio Protech, Inc.

FDA 510(k) clearance K073438 for PROSTIM 1000/2000, Substantially Equivalent on 2008-02-07. Applicant: Bio Protech, Inc.. Device class: 2.

Clearance details

Applicant
Bio Protech, Inc.
Product code
Code GZJ
Device class
Class 2
Regulation
21 CFR 882.5890
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Crofton, MD, US
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