FLUSH DEVICE, AUTOMATIC
FDA 510(k) clearance K851987 · decided 1985-08-16
Clearance details
- K-number
- K851987
- Device name
- FLUSH DEVICE, AUTOMATIC
- Applicant
- Transamerica Delaval, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-05-07
- Decision date
- 1985-08-16
- Days to decision
- 101 days
- Clearance type
- Traditional
- Product code
- DRS
- Device class
- 2
- Regulation number
- 870.2850
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Pasadena, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.