510(k) K833717
K833717 is an FDA 510(k) premarket notification submitted by Advanced Biosearch Assn. for the device "PADGETT SUCTION CANNULA". The FDA issued a decision of Substantially Equivalent on December 14, 1983. The device falls under product code GEA (Cannula, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Advanced Biosearch Assn. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 14, 1983
- Date Received
- October 21, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cannula, Surgical, General & Plastic Surgery
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type