Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Oral/Enteral Syringe with ENFit connector

K-Number: K222772 · 2023-08-17

Decision Date2023-08-17
Product CodePNR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Oral/Enteral Syringe with ENFit connector is a medical device manufactured by Anhui Tiankang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-08-17 under approval number K222772. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Oral/Enteral Syringe with ENFit connector?

Oral/Enteral Syringe with ENFit connector is a medical device that received FDA 510(k) clearance on 2023-08-17. It is manufactured by Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K222772.

When was Oral/Enteral Syringe with ENFit connector approved by the FDA?

Oral/Enteral Syringe with ENFit connector received FDA 510(k) clearance on 2023-08-17, under approval number K222772.

What company makes Oral/Enteral Syringe with ENFit connector?

Oral/Enteral Syringe with ENFit connector is manufactured by Anhui Tiankang Medical Technology Co., Ltd..

What is the FDA product code for Oral/Enteral Syringe with ENFit connector?

The FDA product code for Oral/Enteral Syringe with ENFit connector is PNR.

Other Devices by Anhui Tiankang Medical Technology Co., Ltd.

View all 12 devices →

Related Devices (Code: PNR)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.