510(k) K970468
K970468 is an FDA 510(k) premarket notification submitted by Kinetic Concepts, Inc. for the device "KT AIR BED". The FDA issued a decision of Substantially Equivalent on September 5, 1997. The device falls under product code FNM (Mattress, Air Flotation, Alternating Pressure), a Class II device regulated under 21 CFR 880.5550. Kinetic Concepts, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 5, 1997
- Date Received
- February 7, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mattress, Air Flotation, Alternating Pressure
- Device Class
- Class II
- Regulation Number
- 880.5550
- Review Panel
- HO
- Submission Type