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FDA 510(k)

AUTOPAL 50

K-Number: K021733 · 2002-06-26

ApplicantWieland Dental + Technik GmbH & Co. KG
Decision Date2002-06-26
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AUTOPAL 50 is the device name listed in this FDA 510(k) record. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2002-06-26 under 510(k) number K021733. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOPAL 50?

AUTOPAL 50 is a medical device that received FDA 510(k) clearance on 2002-06-26. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. The 510(k) number is K021733.

When did AUTOPAL 50 receive FDA 510(k) clearance?

AUTOPAL 50 received FDA 510(k) clearance on 2002-06-26, under 510(k) number K021733.

Who is the listed applicant for AUTOPAL 50?

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 AUTOPAL 50?

The FDA product code for AUTOPAL 50 is EJT.

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Other records listing Wieland Dental + Technik GmbH & Co. KG as applicant

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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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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