K911765Substantially Equivalent
Hand Carried Stretcher
L.E. Phillips Career Development Center, Inc., Eau Claire WI / Traditional, Substantially Equivalent
K911765 is the FDA 510(k) clearance record for HAND CARRIED STRETCHER, a class I device, cleared for L.E. Phillips Career Development Center, Inc. on under FDA product code FPP (Stretcher, Hand-Carried). FDA records list one 510(k) clearance for L.E. Phillips Career Development Center, Inc. As of , FDA records show no recalls naming K911765.
Clearance record
- Decision date
- Received
- (56 days to decision)
- Product code
- FPP Stretcher, Hand-Carried
- Regulation
- 21 CFR 880.6900
- Device class
- Class I
- Review panel
- General Hospital
- Applicant
- L.E. Phillips Career Development Center, Inc. 1515 Ball St., Eau Claire WI
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code FPP
Trailing 12 monthsFDA records hold no clearances under product code FPP in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
