GENESIS II, 2.5/5.0 MHZ S.E/5.0MHZ/3.5 16/19 MM AN— 510(k) K873032
Substantially EquivalentBiosound, Inc.
FDA 510(k) clearance K873032 for GENESIS II, 2.5/5.0 MHZ S.E/5.0MHZ/3.5 16/19 MM AN, Substantially Equivalent on 1988-02-18. Applicant: Biosound, Inc.. Device class: 2.
Clearance details
- Applicant
- Biosound, Inc.
- Product code
- Code DXK
- Device class
- Class 2
- Regulation
- 21 CFR 870.2330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
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