Ultra Care Vest Style Body Holder, Small (24455-010,020,030,040,24456-010,020,030,040)
K963561 is the FDA 510(k) clearance record for ULTRA CARE VEST STYLE BODY HOLDER, SMALL (24455-010,020,030,040,24456-010,020,030,040), a class I device, cleared for Tecnol Medical Products, Inc. on under FDA product code FMQ (Restraint, Protective). FDA records list 21 510(k) clearances for Tecnol Medical Products, Inc., from to . As of , FDA records show no recalls naming K963561.
Clearance record
- Decision date
- Received
- (77 days to decision)
- Product code
- FMQ Restraint, Protective
- Regulation
- 21 CFR 880.6760
- Device class
- Class I
- Review panel
- General Hospital
- Applicant
- Tecnol Medical Products, Inc. 7201 Industrial Park Blvd., Fort Worth TX
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code FMQ
Trailing 12 monthsFDA records hold no clearances under product code FMQ 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.
