Flexor Tuohy-Borst Side-Arm Introducer, Ansel Modification; Flexor Check-Flo Introducer, Ansel Modification; Flexor Check-Flo Introducers, Ansel Modification with High-Flex Dilator and Hydrophilic Coating; Flexor Check-Flo Introducer Balkin Up and Over Contralateral Design; Flexor Up and Over Balkin Contralateral Introducer; Flexor Check-Flo Introducer, Raabe Modification; Flexor Check-Flo Performer Introducer
K142829 is the FDA 510(k) clearance record for Flexor Tuohy-Borst Side-Arm Introducer, Ansel Modification; Flexor Check-Flo Introducer, Ansel Modification; Flexor Check-Flo Introducers, Ansel Modification with High-Flex Dilator and Hydrophilic Coating; Flexor Check-Flo Introducer Balkin Up and Over Contralateral Design; Flexor Up and Over Balkin Contralateral Introducer; Flexor Check-Flo Introducer, Raabe Modification; Flexor Check-Flo Performer Introducer, a class II device, cleared for Cook Incorporated on under FDA product code DYB (Introducer, Catheter). FDA records list 279 510(k) clearances for Cook Incorporated, from to . As of , FDA records show 26 recalls naming K142829.
Clearance record
- Decision date
- Received
- (301 days to decision)
- Product code
- DYB Introducer, Catheter
- Regulation
- 21 CFR 870.1340
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Cook Incorporated 750 Daniels Way, Bloomington IN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DYB
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 2 |
| January 2026 | 1 |
| February 2026 | 2 |
| March 2026 | 1 |
| April 2026 | 7 |
| May 2026 | 0 |
| June 2026 | 3 |
| July 2026 | 2 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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