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FDA 510(k)

2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST

K-Number: K851730 · 1985-07-02

ApplicantArtiberia
Decision Date1985-07-02
Product CodeEJY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851730. The device is classified under product code EJY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST?

2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Artiberia. The 510(k) number is K851730.

When did 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST receive FDA 510(k) clearance?

2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851730.

Who is the listed applicant for 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST?

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 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST?

The FDA product code for 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST is EJY.

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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

View all 79 devices →

Related Devices (Code: EJY)

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.

K821787BEACH SURGICAL PLIERS NON-HOOKPacific Dental Corp.

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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