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)

29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY

K-Number: K851789 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product CodeGFJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY 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 K851789. The device is classified under product code GFJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY?

29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851789.

When did 29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY receive FDA 510(k) clearance?

29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851789.

Who is the listed applicant for 29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY?

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 29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY?

The FDA product code for 29-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOY is GFJ.

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 →

Related Devices (Code: GFJ)

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.

K844017MICROTENS 7757 T.E.N.S. STIMULATORRabar, Inc.K822204ENT MALLETSKelleher 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.

↑