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FDA 510(k)

SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5

K-Number: K031065 · 2003-06-23

ApplicantSyringex Medical, Inc.
Decision Date2003-06-23
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5 is the device name listed in this FDA 510(k) record. The listed applicant is Syringex Medical, Inc.. It received FDA 510(k) clearance on 2003-06-23 under 510(k) number K031065. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5?

SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5 is a medical device that received FDA 510(k) clearance on 2003-06-23. The listed applicant is Syringex Medical, Inc.. The 510(k) number is K031065.

When did SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5 receive FDA 510(k) clearance?

SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5 received FDA 510(k) clearance on 2003-06-23, under 510(k) number K031065.

Who is the listed applicant for SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5?

The FDA 510(k) record lists Syringex Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5?

The FDA product code for SYRINGEX SAFETY SYRINGE, MODEL 0322G1.5 is MEG.

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Related Devices (Code: MEG)

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Official Source

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

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