MODEL 102 PH METER
FDA 510(k) clearance K870811 · decided 1987-03-24
Clearance details
- K-number
- K870811
- Device name
- MODEL 102 PH METER
- Applicant
- Mesa Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-03-03
- Decision date
- 1987-03-24
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- LRI
- Device class
- 2
- Regulation number
- 876.5820
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Wheat Ridge, CO, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.