510(k) K942529
K942529 is an FDA 510(k) premarket notification submitted by Health Care Contracts, Inc. for the device "HCI TUBE STABILIZER". The FDA issued a decision of Substantially Equivalent on June 14, 1995. 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
- June 14, 1995
- Date Received
- May 27, 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