STUDIODOP VICORDER
FDA 510(k) clearance K071730 · decided 2007-12-20
Clearance details
- K-number
- K071730
- Device name
- STUDIODOP VICORDER
- Applicant
- Skidmore Medical, Limited
- Decision
- Substantially Equivalent
- Date received
- 2007-06-25
- Decision date
- 2007-12-20
- Days to decision
- 178 days
- Clearance type
- Abbreviated
- Product code
- JOP
- Device class
- 2
- Regulation number
- 870.2880
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Evergreen, CO, US
- Third-party review
- No
- Expedited review
- No
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| SPECTRADOP (K925078) | Bennett and Assoc., Inc. | 1995-07-17 |
| REUSABLE CW DOPPLER PROBES: MODELS P8M05S8A, P8M05N5A, & LCW-8 (K934638) | Koven Technology, Inc. | 1994-05-13 |
| MODEL HD-207 BIDIRECTIONAL VELOCITY METER (K912409) | Koven and Assoc., Inc. | 1991-12-23 |
Recalls involving this device
No recalls on record reference this clearance.