ZOLL PROPAQ MD
FDA 510(k) clearance K100654 · decided 2010-07-29
Clearance details
- K-number
- K100654
- Device name
- ZOLL PROPAQ MD
- Applicant
- Zoll Medical Corporation, World Wide Headquarters
- Decision
- Substantially Equivalent
- Date received
- 2010-03-08
- Decision date
- 2010-07-29
- Days to decision
- 143 days
- Clearance type
- Traditional
- Product code
- LDD
- Device class
- 2
- Regulation number
- 870.5300
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Chelsmford, MA, US
- Third-party review
- No
- Expedited review
- No
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| ZOLL R SERIES (K081574) | ZOLL Medical Corporation | 2008-09-18 |
Recalls involving this device
No recalls on record reference this clearance.