600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI
K-Number: K851712 · 1985-06-11
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Device Summary
Frequently Asked Questions
What is the 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI?
600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Artiberia. The 510(k) number is K851712.
When did 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI receive FDA 510(k) clearance?
600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851712.
Who is the listed applicant for 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI?
The FDA 510(k) record lists Artiberia as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI?
The FDA product code for 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI is EMG.
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 Artiberia 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: EMG)
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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