PHONOANGIOGRAPHIC SPECTRAL ANALYZER— 510(k) K840169
Substantially EquivalentBiotronics Instruments
FDA 510(k) clearance K840169 for PHONOANGIOGRAPHIC SPECTRAL ANALYZER, Substantially Equivalent on 1985-03-01. Applicant: Biotronics Instruments. Device class: 2.
Clearance details
- Applicant
- Biotronics Instruments
- Product code
- Product code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wauwatosa, WI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.