PULSAIR MODEL SP-1— 510(k) K832177
Substantially EquivalentThermowave Medical Device Corp.
FDA 510(k) clearance K832177 for PULSAIR MODEL SP-1, Substantially Equivalent on 1983-12-09. Applicant: Thermowave Medical Device Corp.. Device class: 1.
Clearance details
- Applicant
- Thermowave Medical Device Corp.
- Product code
- Code IRQ
- Device class
- Class 1
- Regulation
- 21 CFR 890.5950
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code IRQ
view allData sourced from openFDA. This site is unofficial and independent of the FDA.