510(k) K896730
K896730 is an FDA 510(k) premarket notification submitted by Unoplast A/S for the device "SUCTION CATHETER STRAIGHT/COUDE". The FDA issued a decision of Substantially Equivalent on Mar 30, 1990. The device falls under product code BSY (Catheters, Suction, Tracheobronchial), a Class I device regulated under 21 CFR 868.6810. Unoplast A/S has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 30, 1990
- Date Received
- Nov 30, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheters, Suction, Tracheobronchial
- Device Class
- Class I
- Regulation Number
- 868.6810
- Review Panel
- AN
- Submission Type