SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE
K-Number: K031716 · 2003-07-10
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Device Summary
Frequently Asked Questions
What is the SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE?
SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE is a medical device that received FDA 510(k) clearance on 2003-07-10. The listed applicant is Asia-Med GmbH and CO KG. The 510(k) number is K031716.
When did SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE receive FDA 510(k) clearance?
SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE received FDA 510(k) clearance on 2003-07-10, under 510(k) number K031716.
Who is the listed applicant for SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE?
The FDA 510(k) record lists Asia-Med GmbH and CO KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE?
The FDA product code for SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE is MQX.
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 Asia-Med GmbH and CO KG 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: MQX)
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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