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FDA 510(k)

PRESS TACK NEEDLE

K-Number: K042063 · 2004-10-14

ApplicantAsia-Med GmbH & Co. Kg. - Werk Suhl
Decision Date2004-10-14
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRESS TACK NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Asia-Med GmbH & Co. Kg. - Werk Suhl. It received FDA 510(k) clearance on 2004-10-14 under 510(k) number K042063. 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 PRESS TACK NEEDLE?

PRESS TACK NEEDLE is a medical device that received FDA 510(k) clearance on 2004-10-14. The listed applicant is Asia-Med GmbH & Co. Kg. - Werk Suhl. The 510(k) number is K042063.

When did PRESS TACK NEEDLE receive FDA 510(k) clearance?

PRESS TACK NEEDLE received FDA 510(k) clearance on 2004-10-14, under 510(k) number K042063.

Who is the listed applicant for PRESS TACK NEEDLE?

The FDA 510(k) record lists Asia-Med GmbH & Co. Kg. - Werk Suhl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESS TACK NEEDLE?

The FDA product code for PRESS TACK NEEDLE is MQX.

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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.

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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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