CHEETAH I.V.D.S., MODEL 2002P
FDA 510(k) clearance K023370 · decided 2002-12-24
Clearance details
- K-number
- K023370
- Device name
- CHEETAH I.V.D.S., MODEL 2002P
- Applicant
- Cheetah Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2002-10-08
- Decision date
- 2002-12-24
- Days to decision
- 77 days
- Clearance type
- Traditional
- Product code
- DQK
- Device class
- 2
- Regulation number
- 870.1425
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Ra'Ananna 43373, IL
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.