CONPHAR SUPERTONE STETHOSCOPE— 510(k) K801189
Substantially EquivalentConphar, Inc.
FDA 510(k) clearance K801189 for CONPHAR SUPERTONE STETHOSCOPE, Substantially Equivalent on 1980-06-04. Applicant: Conphar, Inc.. Device class: 2.
Clearance details
- Applicant
- Conphar, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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