MYOPULSE— 510(k) K833928
Substantially EquivalentBiomedical Design Instruments
FDA 510(k) clearance K833928 for MYOPULSE, Substantially Equivalent on 1984-12-14. Applicant: Biomedical Design Instruments.
Clearance details
- Applicant
- Biomedical Design Instruments
- Product code
- Code IPF
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.