Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

13-440 TO 13-464 VARIOUS DISSECTING SCISSORS

K-Number: K851765 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product Code
DecisionSubstantially Equivalent

Device Summary

13-440 TO 13-464 VARIOUS DISSECTING SCISSORS 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 K851765. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 13-440 TO 13-464 VARIOUS DISSECTING SCISSORS?

13-440 TO 13-464 VARIOUS DISSECTING SCISSORS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851765.

When did 13-440 TO 13-464 VARIOUS DISSECTING SCISSORS receive FDA 510(k) clearance?

13-440 TO 13-464 VARIOUS DISSECTING SCISSORS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851765.

Who is the listed applicant for 13-440 TO 13-464 VARIOUS DISSECTING SCISSORS?

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 →

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.

↑