TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML)
K-Number: K023458 · 2002-11-07
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Device Summary
Frequently Asked Questions
What is the TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML)?
TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML) is a medical device that received FDA 510(k) clearance on 2002-11-07. The listed applicant is Taiject Medical Device Co., Ltd.. The 510(k) number is K023458.
When did TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML) receive FDA 510(k) clearance?
TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML) received FDA 510(k) clearance on 2002-11-07, under 510(k) number K023458.
Who is the listed applicant for TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML)?
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 (FA14 SERIES 10ML/FA15 SERIES 20ML)?
The FDA product code for TMD SAFETY SYRINGE (FA14 SERIES 10ML/FA15 SERIES 20ML) 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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