Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes with Accessories for Power Injectors (900103H); Disposable Syringes with Accessories for Power Injectors (801800H); Disposable Syringes with Accessories for Power Injectors (800099T); Disposable Syringes with Accessories for Power Injectors (800099H); Disposable Syringes with Accessories for Power Injectors (800096T); Disposable Syringes with Accessories for Power Injectors (800096H); Disposable Syr
K252652 is the FDA 510(k) clearance record for Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes with Accessories for Power Injectors (900103H); Disposable Syringes with Accessories for Power Injectors (801800H); Disposable Syringes with Accessories for Power Injectors (800099T); Disposable Syringes with Accessories for Power Injectors (800099H); Disposable Syringes with Accessories for Power Injectors (800096T); Disposable Syringes with Accessories for Power Injectors (800096H); Disposable Syr, a class II device, cleared for Fortis Biosolutions Company Limited on under FDA product code DXT (Injector And Syringe, Angiographic). FDA records list one 510(k) clearance for Fortis Biosolutions Company Limited. As of , FDA records show no recalls naming K252652.
Clearance record
- Decision date
- Received
- (265 days to decision)
- Product code
- DXT Injector And Syringe, Angiographic
- Regulation
- 21 CFR 870.1650
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Fortis Biosolutions Company Limited # 121, Ln. 215, Gaoyang S. Rd., Taoyuan City, TW
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DXT
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 3 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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