HEARTSTREAM FR2 AED, MODEL M3860A,M3861A
FDA 510(k) clearance K003565 · decided 2000-12-20
Clearance details
- K-number
- K003565
- Device name
- HEARTSTREAM FR2 AED, MODEL M3860A,M3861A
- Applicant
- Agilent Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2000-11-20
- Decision date
- 2000-12-20
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- MKJ
- Device class
- 3
- Regulation number
- 870.5310
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Seattle, WA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Agilent Technologies
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| MMR IHC Panel pharmDx (Dako Omnis) (P250004) | Agilent Technologies, Inc. | 2025-08-15 |
| PD-L1 IHC 22C3 pharmDx (Dako Omnis) (P150013/S028) | Agilent Technologies, Inc. | 2025-08-04 |
| PD-L1 IHC 28-8 pharmDx (P150025/S017) | Agilent Technologies, Inc. | 2025-06-27 |
| MAGE-A4 IHC 1F9 pharmDx (P230016/S002) | Agilent Technologies, Inc. | 2025-06-27 |
| PD-L1 IHC 22C3 PHARMDX (P150013/S030) | Agilent Technologies, Inc. | 2025-06-27 |
| Ki-67 IHC MIB-1 pharmDx (Dako Omnis) (P210026/S002) | Agilent Technologies, Inc. | 2025-02-28 |
| PD-L1 IHC 22C3 pharmDx (P150013/S029) | Agilent Technologies, Inc. | 2025-02-28 |
| MAGE-A4 IHC 1F9 pharmDx (P230016/S001) | Agilent Technologies, Inc. | 2025-02-28 |