ACCESSORY TO GENESIS III (GCFM)— 510(k) K913209
Substantially EquivalentBiosound, Inc.
FDA 510(k) clearance K913209 for ACCESSORY TO GENESIS III (GCFM), Substantially Equivalent on 1992-05-15. 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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More clearances from Biosound, Inc.
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