K252483 is the FDA 510(k) clearance record for Enteral Syringe (20ml, 60ml), a class II device, cleared for Chirana T.Injecta,A.S. on 2026-07-01 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 2 510(k) clearances for Chirana T.Injecta,A.S., from 2026-04-17 to 2026-07-01 . As of 2026-09-10 , FDA records show no recalls naming K252483.
Clearance record Decision date 2026-07-01 Received 2025-08-07 (328 days to decision) Product code PNR Enteral Syringes With Enteral Specific ConnectorsRegulation 21 CFR 876.5980 Device class Class II Review panel Gastroenterology, Urology Applicant Chirana T.Injecta,A.S. Nám.Dr.A.Schweitzera 194, Stará Turá, SK 510(k) summary Summary PDF ↗ Third party review No
Clearances, product code PNR Trailing 12 months 2 clearances under product code PNR in the twelve months to October 2026, April 2026 the highest month at 1. Show the numbers 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.
Product code PNR
Z-0850-2024 Class I The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility... Cardinal Health 200, LLC / initiated 2023-12-28 / 397676 units Z-0849-2024 Class I The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility... Cardinal Health 200, LLC / initiated 2023-12-28 / 223056 units Z-0848-2024 Class I The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility... Cardinal Health 200, LLC / initiated 2023-12-28 / 60760 units Z-0847-2024 Class I The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility... Cardinal Health 200, LLC / initiated 2023-12-28 / 20186 units
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About this record Sourced from the FDA 510(k) premarket notification database, ingested from openFDA. MDM adds the decision time in days, the product code cross-link, recalls sharing that product code, and MDM coverage of the record.
Predicate devices are not listed. The openFDA 510(k) endpoint does not publish predicate references, so MDM does not assert them. Where a 510(k) summary exists, the FDA PDF is linked above and names the predicate itself.
Data as of 2026-09-28 , the FDA export date for this dataset. Page last changed 2026-09-05 . View this record on fda.gov ↗ (opens on fda.gov)