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FDA 510(k)

500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA

K-Number: K851708 · 1985-07-01

ApplicantArtiberia
Decision Date1985-07-01
Product CodeEMG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-01 under 510(k) number K851708. The device is classified under product code EMG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA?

500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Artiberia. The 510(k) number is K851708.

When did 500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA receive FDA 510(k) clearance?

500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA received FDA 510(k) clearance on 1985-07-01, under 510(k) number K851708.

Who is the listed applicant for 500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA?

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 500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA?

The FDA product code for 500/1 TO 500/80 VARIOUS TYPES OF ENGLISH PAT DENTA 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.

View all 79 devices →

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

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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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