MAMMOSITE MULTI LUMEN— 510(k) K092405
UnknownHologic, Inc.
FDA 510(k) clearance K092405 for MAMMOSITE MULTI LUMEN, Unknown on 2009-08-27. Applicant: Hologic, Inc.. Device class: 2.
Clearance details
- Applicant
- Hologic, Inc.
- Product code
- Code JAQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Special
- Location
- Marlborough, MA, US
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