510(k) K940448
K940448 is an FDA 510(k) premarket notification submitted by Medical Accessory Services, Inc. for the device "NETOH ENDOTRACHEAL TUBE HOLDER". The FDA issued a decision of Substantially Equivalent on February 22, 1994. The device falls under product code CBH (Device, Fixation, Tracheal Tube), a Class I device regulated under 21 CFR 868.5770.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 22, 1994
- Date Received
- February 1, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Fixation, Tracheal Tube
- Device Class
- Class I
- Regulation Number
- 868.5770
- Review Panel
- AN
- Submission Type