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FDA 510(k)

SAFEPRO PLUS SAFETY SYRINGE

K-Number: K031830 · 2003-08-05

Decision Date2003-08-05
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFEPRO PLUS SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Formosa Medical Devices, Inc.. It received FDA 510(k) clearance on 2003-08-05 under 510(k) number K031830. 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 SAFEPRO PLUS SAFETY SYRINGE?

SAFEPRO PLUS SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2003-08-05. The listed applicant is Formosa Medical Devices, Inc.. The 510(k) number is K031830.

When did SAFEPRO PLUS SAFETY SYRINGE receive FDA 510(k) clearance?

SAFEPRO PLUS SAFETY SYRINGE received FDA 510(k) clearance on 2003-08-05, under 510(k) number K031830.

Who is the listed applicant for SAFEPRO PLUS SAFETY SYRINGE?

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

What is the FDA product code for SAFEPRO PLUS SAFETY SYRINGE?

The FDA product code for SAFEPRO PLUS SAFETY SYRINGE is MEG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Formosa Medical Devices, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: MEG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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