LARGE FACE ANEROID SPHYGMOMANOMETER, WALL MODEL, DESK MODEL, MOBILE STAND MODEL, MODEL 41XX, 42XX, 43XX
FDA 510(k) clearance K092604 · decided 2009-10-21
Clearance details
- K-number
- K092604
- Device name
- LARGE FACE ANEROID SPHYGMOMANOMETER, WALL MODEL, DESK MODEL, MOBILE STAND MODEL, MODEL 41XX, 42XX, 43XX
- Applicant
- Trimline Medical Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 2009-08-25
- Decision date
- 2009-10-21
- Days to decision
- 57 days
- Clearance type
- Abbreviated
- Product code
- DXQ
- Device class
- 2
- Regulation number
- 870.1120
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Branchburg, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.