510(k) K925020
K925020 is an FDA 510(k) premarket notification submitted by Customed, Inc. for the device "TRACHEOSTOMY CARE KIT (STERILE)". The FDA issued a decision of Substantially Equivalent (kit) on July 7, 1993. The device falls under product code JOH (Tube Tracheostomy And Tube Cuff), a Class II device regulated under 21 CFR 868.5800. Customed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESK (Substantially Equivalent (kit))
- Decision Date
- July 7, 1993
- Date Received
- September 24, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube Tracheostomy And Tube Cuff
- Device Class
- Class II
- Regulation Number
- 868.5800
- Review Panel
- AN
- Submission Type