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FDA 510(k)

1CC FUTURA SAFETY SYRINGE

K-Number: K023323 · 2002-10-29

Decision Date2002-10-29
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

1CC FUTURA SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Futura Medical Technology. It received FDA 510(k) clearance on 2002-10-29 under 510(k) number K023323. 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 1CC FUTURA SAFETY SYRINGE?

1CC FUTURA SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2002-10-29. The listed applicant is Futura Medical Technology. The 510(k) number is K023323.

When did 1CC FUTURA SAFETY SYRINGE receive FDA 510(k) clearance?

1CC FUTURA SAFETY SYRINGE received FDA 510(k) clearance on 2002-10-29, under 510(k) number K023323.

Who is the listed applicant for 1CC FUTURA SAFETY SYRINGE?

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

What is the FDA product code for 1CC FUTURA SAFETY SYRINGE?

The FDA product code for 1CC FUTURA 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.

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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