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FDA 510(k)

SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE

K-Number: K031716 · 2003-07-10

Decision Date2003-07-10
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Asia-Med GmbH and CO KG. It received FDA 510(k) clearance on 2003-07-10 under 510(k) number K031716. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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