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FDA 510(k)

13-170 DEAVER SCISSOR, TWO SIZES

K-Number: K851755 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product Code
DecisionSubstantially Equivalent

Device Summary

13-170 DEAVER SCISSOR, TWO SIZES 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 K851755. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 13-170 DEAVER SCISSOR, TWO SIZES?

13-170 DEAVER SCISSOR, TWO SIZES is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851755.

When did 13-170 DEAVER SCISSOR, TWO SIZES receive FDA 510(k) clearance?

13-170 DEAVER SCISSOR, TWO SIZES received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851755.

Who is the listed applicant for 13-170 DEAVER SCISSOR, TWO SIZES?

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

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.

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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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