510(k) K932260
K932260 is an FDA 510(k) premarket notification submitted by Ferno for the device "FERNO-WASHINGTON AMBULANCE COT, 93ES SQUAD-MATE". The FDA issued a decision of Substantially Equivalent on September 9, 1993. The device falls under product code FPO (Stretcher, Wheeled), a Class II device regulated under 21 CFR 880.6910. Ferno has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 9, 1993
- Date Received
- April 20, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stretcher, Wheeled
- Device Class
- Class II
- Regulation Number
- 880.6910
- Review Panel
- HO
- Submission Type