HD Steth— 510(k) K201299
Substantially EquivalentHd Medical, Inc.
FDA 510(k) clearance K201299 for HD Steth, Substantially Equivalent on 2020-07-10. Applicant: Hd Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Hd Medical, 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
- Santa Clara, CA, US
Recent devices under product code DQD
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