CONPHAR DUAL HEAD STETHOSCOPE— 510(k) K801183
Substantially EquivalentConphar, Inc.
FDA 510(k) clearance K801183 for CONPHAR DUAL HEAD STETHOSCOPE, Substantially Equivalent on 1980-06-04. Applicant: Conphar, Inc.. Device class: 1.
Clearance details
- Applicant
- Conphar, Inc.
- Product code
- Code LDE
- Device class
- Class 1
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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