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FDA 510(k)

3CC NMT SAFETY SYRINGE

K-Number: K010819 · 2001-11-08

Decision Date2001-11-08
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3CC NMT SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is New Medical Technology , Ltd.. It received FDA 510(k) clearance on 2001-11-08 under 510(k) number K010819. 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 3CC NMT SAFETY SYRINGE?

3CC NMT SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2001-11-08. The listed applicant is New Medical Technology , Ltd.. The 510(k) number is K010819.

When did 3CC NMT SAFETY SYRINGE receive FDA 510(k) clearance?

3CC NMT SAFETY SYRINGE received FDA 510(k) clearance on 2001-11-08, under 510(k) number K010819.

Who is the listed applicant for 3CC NMT SAFETY SYRINGE?

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

What is the FDA product code for 3CC NMT SAFETY SYRINGE?

The FDA product code for 3CC NMT 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 New Medical Technology , Ltd. 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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