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FDA 510(k)

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

K-Number: K022278 · 2002-09-12

Decision Date2002-09-12
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML) is the device name listed in this FDA 510(k) record. The listed applicant is Taiject Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2002-09-12 under 510(k) number K022278. 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 TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)?

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML) is a medical device that received FDA 510(k) clearance on 2002-09-12. The listed applicant is Taiject Medical Device Co., Ltd.. The 510(k) number is K022278.

When did TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML) receive FDA 510(k) clearance?

TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML) received FDA 510(k) clearance on 2002-09-12, under 510(k) number K022278.

Who is the listed applicant for TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)?

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

What is the FDA product code for TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)?

The FDA product code for TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML) 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 Taiject Medical Device Co., 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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