CANNULA CLAMP
FDA 510(k) clearance K771419 · decided 1977-08-26
Clearance details
- K-number
- K771419
- Device name
- CANNULA CLAMP
- Applicant
- Quinton, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-08-01
- Decision date
- 1977-08-26
- Days to decision
- 25 days
- Clearance type
- Traditional
- Product code
- FKC
- Device class
- 1
- Regulation number
- 876.5540
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.