PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH— 510(k) K832374
Substantially EquivalentSonicaid, Inc.
FDA 510(k) clearance K832374 for PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH, Substantially Equivalent on 1983-12-01. Applicant: Sonicaid, Inc..
Clearance details
- Applicant
- Sonicaid, Inc.
- Product code
- Code JOM
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.