CARDIOSONIC ACOUSTIC AMPLIFIER— 510(k) K813510
Substantially EquivalentSrs Co.
FDA 510(k) clearance K813510 for CARDIOSONIC ACOUSTIC AMPLIFIER, Substantially Equivalent on 1982-01-12. Applicant: Srs Co..
Clearance details
- Applicant
- Srs Co.
- Product code
- Code LDE
- 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.