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FDA 510(k)

Pre-Filled Normal Saline Flush Syringe

K-Number: K223584 · 2023-08-12

ApplicantAnhui Tianyang Pharmaceutical Co., Ltd.
Decision Date2023-08-12
Product CodeNGT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Pre-Filled Normal Saline Flush Syringe is a medical device manufactured by Anhui Tianyang Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2023-08-12 under approval number K223584. The device is classified under product code NGT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pre-Filled Normal Saline Flush Syringe?

Pre-Filled Normal Saline Flush Syringe is a medical device that received FDA 510(k) clearance on 2023-08-12. It is manufactured by Anhui Tianyang Pharmaceutical Co., Ltd.. The 510(k) number is K223584.

When was Pre-Filled Normal Saline Flush Syringe approved by the FDA?

Pre-Filled Normal Saline Flush Syringe received FDA 510(k) clearance on 2023-08-12, under approval number K223584.

What company makes Pre-Filled Normal Saline Flush Syringe?

Pre-Filled Normal Saline Flush Syringe is manufactured by Anhui Tianyang Pharmaceutical Co., Ltd..

What is the FDA product code for Pre-Filled Normal Saline Flush Syringe?

The FDA product code for Pre-Filled Normal Saline Flush Syringe is NGT.

Related Clinical Trials

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Related Devices (Code: NGT)

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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.

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