DIRECTVISION CATHETER, UNCOATED
FDA 510(k) clearance K110214 · decided 2011-05-27
Clearance details
- K-number
- K110214
- Device name
- DIRECTVISION CATHETER, UNCOATED
- Applicant
- Percuvision
- Decision
- Substantially Equivalent
- Date received
- 2011-01-25
- Decision date
- 2011-05-27
- Days to decision
- 122 days
- Clearance type
- Special
- Product code
- EZL
- Device class
- 2
- Regulation number
- 876.5130
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Ashland, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.