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FDA 510(k)

23-130 TO 23-144 TWO TYPES OF DIRECTORS

K-Number: K851778 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product Code
DecisionSubstantially Equivalent

Device Summary

23-130 TO 23-144 TWO TYPES OF DIRECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-20 under 510(k) number K851778. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 23-130 TO 23-144 TWO TYPES OF DIRECTORS?

23-130 TO 23-144 TWO TYPES OF DIRECTORS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851778.

When did 23-130 TO 23-144 TWO TYPES OF DIRECTORS receive FDA 510(k) clearance?

23-130 TO 23-144 TWO TYPES OF DIRECTORS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851778.

Who is the listed applicant for 23-130 TO 23-144 TWO TYPES OF DIRECTORS?

The FDA 510(k) record lists Artiberia as the applicant. This does not by itself establish the device manufacturer.

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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.

K8517451-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON BK85178627-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

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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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