ACKRAD SIALOGRAPHY CATHETER
FDA 510(k) clearance K852154 · decided 1985-06-26
Clearance details
- K-number
- K852154
- Device name
- ACKRAD SIALOGRAPHY CATHETER
- Applicant
- Ackrad Laboratories
- Decision
- Substantially Equivalent
- Date received
- 1985-05-17
- Decision date
- 1985-06-26
- Days to decision
- 40 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Cranford, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.