Monoject™ Enteral Syringe with ENFit Connector (401SE); Monoject™ Enteral Syringe with ENFit Connector (403SE); Monoject™ Enteral Syringe with ENFit Connector (406SE); Monoject™ Enteral Syringe with ENFit Connector (412SE); Monoject™ Enteral Syringe with ENFit Connector (435SE); Monoject™ Enteral Syringe with ENFit Connector (460SE)
K243652 is the FDA 510(k) clearance record for Monoject™ Enteral Syringe with ENFit Connector (401SE); Monoject™ Enteral Syringe with ENFit Connector (403SE); Monoject™ Enteral Syringe with ENFit Connector (406SE); Monoject™ Enteral Syringe with ENFit Connector (412SE); Monoject™ Enteral Syringe with ENFit Connector (435SE); Monoject™ Enteral Syringe with ENFit Connector (460SE), a class II device, cleared for Cardinalhealth on under FDA product code PNR (Enteral Syringes With Enteral Specific Connectors). FDA's definition for product code PNR reads: "Delivers nutrition, medication, or hydration orally or to a gastrointestinal tube or extension set using AAMI/CN3(PS):2014 compliant connectors". FDA records list 32 510(k) clearances for Cardinalhealth, from to . As of , FDA records show no recalls naming K243652.
Clearance record
- Decision date
- Received
- (23 days to decision)
- Product code
- PNR Enteral Syringes With Enteral Specific Connectors
- Regulation
- 21 CFR 876.5980
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Applicant
- Cardinalhealth 3651 Birchwood Dr., Waukegan IL
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code PNR
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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