IMPULSE 6000D/7000DP— 510(k) K072114
Substantially EquivalentFluke Biomedical
FDA 510(k) clearance K072114 for IMPULSE 6000D/7000DP, Substantially Equivalent on 2008-01-28. Applicant: Fluke Biomedical. Device class: 2.
Clearance details
- Applicant
- Fluke Biomedical
- Product code
- Code DRL
- Device class
- Class 2
- Regulation
- 21 CFR 870.5325
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Orange, CA, US
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