PROSTIM 1000/2000— 510(k) K073438
Substantially EquivalentBio 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.