510(k) K862666
K862666 is an FDA 510(k) premarket notification submitted by Mallinckrodt Critical Care for the device "UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)". The FDA issued a decision of Substantially Equivalent on August 1, 1986. The device falls under product code BTR (Tube, Tracheal (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5730. Mallinckrodt Critical Care has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 1, 1986
- Date Received
- July 14, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Tracheal (W/Wo Connector)
- Device Class
- Class II
- Regulation Number
- 868.5730
- Review Panel
- AN
- Submission Type