FLEXIBLE FIBEROPTIC ENDOSCOPE
FDA 510(k) clearance K850393 · decided 1985-06-04
Clearance details
- K-number
- K850393
- Device name
- FLEXIBLE FIBEROPTIC ENDOSCOPE
- Applicant
- Microvasive
- Decision
- Substantially Equivalent
- Date received
- 1985-02-01
- Decision date
- 1985-06-04
- Days to decision
- 123 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Milford, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.