VAN DELLEN CANNULA
FDA 510(k) clearance K873464 · decided 1987-11-23
Clearance details
- K-number
- K873464
- Device name
- VAN DELLEN CANNULA
- Applicant
- Van Dellen, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1987-08-28
- Decision date
- 1987-11-23
- Days to decision
- 87 days
- Clearance type
- Traditional
- Product code
- JOL
- Device class
- 2
- Regulation number
- 880.6740
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Tucson, AZ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.