ENDOGUIDE
FDA 510(k) clearance K063654 · decided 2007-01-31
Clearance details
- K-number
- K063654
- Device name
- ENDOGUIDE
- Applicant
- Kms Medical, LLC
- Decision
- Substantially Equivalent
- Date received
- 2006-12-08
- Decision date
- 2007-01-31
- Days to decision
- 54 days
- Clearance type
- Traditional
- Product code
- FDF
- Device class
- 2
- Regulation number
- 876.1500
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Miami, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.