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FDA 510(k)

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK

K-Number: K851763 · 1985-06-11

ApplicantArtiberia
Decision Date1985-06-11
Product CodeKBD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K851763. The device is classified under product code KBD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK?

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Artiberia. The 510(k) number is K851763.

When did 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK receive FDA 510(k) clearance?

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851763.

Who is the listed applicant for 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK?

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 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK?

The FDA product code for 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK is KBD.

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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: KBD)

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.

K822524EAR SPOONKelleher Corp.K791124SURGICAL SCISSORSXomed, Inc.

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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