MDP2000 MEDICAL DATA PROCESSOR
FDA 510(k) clearance K972880 · decided 1997-10-22
Clearance details
- K-number
- K972880
- Device name
- MDP2000 MEDICAL DATA PROCESSOR
- Applicant
- Vidco, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1997-08-05
- Decision date
- 1997-10-22
- Days to decision
- 78 days
- Clearance type
- Traditional
- Product code
- MSX
- Device class
- 2
- Regulation number
- 870.2300
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Beaverton, OR, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, o recall (Z-0582-2016) | Vidco, Inc. | 2016-01-04 |