DUOPRO SAFETY SYRINGE (DUOPROSS)
K-Number: K022806 · 2002-09-19
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Device Summary
Frequently Asked Questions
What is the DUOPRO SAFETY SYRINGE (DUOPROSS)?
DUOPRO SAFETY SYRINGE (DUOPROSS) is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is M.K. Meditech Co. , Ltd.. The 510(k) number is K022806.
When did DUOPRO SAFETY SYRINGE (DUOPROSS) receive FDA 510(k) clearance?
DUOPRO SAFETY SYRINGE (DUOPROSS) received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022806.
Who is the listed applicant for DUOPRO SAFETY SYRINGE (DUOPROSS)?
The FDA 510(k) record lists M.K. Meditech Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUOPRO SAFETY SYRINGE (DUOPROSS)?
The FDA product code for DUOPRO SAFETY SYRINGE (DUOPROSS) 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 M.K. Meditech 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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