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)

Plastic LOR Syringe

K-Number: K201356 · 2021-02-12

Decision Date2021-02-12
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Plastic LOR Syringe is a medical device manufactured by Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2021-02-12 under approval number K201356. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Plastic LOR Syringe?

Plastic LOR Syringe is a medical device that received FDA 510(k) clearance on 2021-02-12. It is manufactured by Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K201356.

When was Plastic LOR Syringe approved by the FDA?

Plastic LOR Syringe received FDA 510(k) clearance on 2021-02-12, under approval number K201356.

What company makes Plastic LOR Syringe?

Plastic LOR Syringe is manufactured by Jiangsu Caina Medical Co.,Ltd.

What is the FDA product code for Plastic LOR Syringe?

The FDA product code for Plastic LOR Syringe is CAZ.

Other Devices by Jiangsu Caina Medical Co.,Ltd

View all 15 devices →

Related Devices (Code: CAZ)

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.