MEDILOG PH1
FDA 510(k) clearance K840934 · decided 1984-06-28
Clearance details
- K-number
- K840934
- Device name
- MEDILOG PH1
- Applicant
- Oxford Medilog, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-03-05
- Decision date
- 1984-06-28
- Days to decision
- 115 days
- Clearance type
- Traditional
- Product code
- EXW
- Device class
- 2
- Regulation number
- 876.1725
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Coral Gables, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.