AUROPAL SOLDER W-2
K-Number: K022451 · 2002-09-11
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Device Summary
Frequently Asked Questions
What is the AUROPAL SOLDER W-2?
AUROPAL SOLDER W-2 is a medical device that received FDA 510(k) clearance on 2002-09-11. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. The 510(k) number is K022451.
When did AUROPAL SOLDER W-2 receive FDA 510(k) clearance?
AUROPAL SOLDER W-2 received FDA 510(k) clearance on 2002-09-11, under 510(k) number K022451.
Who is the listed applicant for AUROPAL SOLDER W-2?
The FDA 510(k) record lists Wieland Dental + Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUROPAL SOLDER W-2?
The FDA product code for AUROPAL SOLDER W-2 is EJT.
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 Wieland Dental + Technik GmbH & 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: EJT)
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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