Profoject™ Low Dead Space Syringe /Profoject™ Tuberculin Syringe; Profoject™ Low Dead Space Syringe with Needle /Profoject™ Tuberculin Syringe with Needle; Profoject™ Low Dead Space Syringe with Permanent Needle /Profoject™ Tuberculin Syringe with Permanent Needle; Profoject™ Low Dead Space Safety Syringe /Profoject™ Tuberculin Safety Syringe
K252814 is the FDA 510(k) clearance record for Profoject™ Low Dead Space Syringe /Profoject™ Tuberculin Syringe; Profoject™ Low Dead Space Syringe with Needle /Profoject™ Tuberculin Syringe with Needle; Profoject™ Low Dead Space Syringe with Permanent Needle /Profoject™ Tuberculin Syringe with Permanent Needle; Profoject™ Low Dead Space Safety Syringe /Profoject™ Tuberculin Safety Syringe, a class II device, cleared for CMT Health PTE., Ltd. on under FDA product code QNQ (Low Dead Space Piston Syringe). FDA's definition for product code QNQ reads: "A low dead space syringe is a piston syringe designed to reduce medication waste. The device consists of a calibrated hollow barrel, a moveable plunger, and may include a needle. The device can be used by health care professions or for...". FDA records list 10 510(k) clearances for CMT Health PTE., Ltd., from to . As of , FDA records show no recalls naming K252814.
Clearance record
- Decision date
- Received
- (168 days to decision)
- Product code
- QNQ Low Dead Space Piston Syringe
- Regulation
- 21 CFR 880.5860
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- CMT Health PTE., Ltd. 150 Beach Rd., #28-05, Gateway W., Singapore, SG
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code QNQ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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