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)

17-900 TO 17-980 VARIOUS TOWEL CLAMPS

K-Number: K851774 · 1985-06-20

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

Device Summary

17-900 TO 17-980 VARIOUS TOWEL CLAMPS 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 K851774. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 17-900 TO 17-980 VARIOUS TOWEL CLAMPS?

17-900 TO 17-980 VARIOUS TOWEL CLAMPS is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851774.

When did 17-900 TO 17-980 VARIOUS TOWEL CLAMPS receive FDA 510(k) clearance?

17-900 TO 17-980 VARIOUS TOWEL CLAMPS received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851774.

Who is the listed applicant for 17-900 TO 17-980 VARIOUS TOWEL CLAMPS?

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 17-900 TO 17-980 VARIOUS TOWEL CLAMPS?

The FDA product code for 17-900 TO 17-980 VARIOUS TOWEL CLAMPS is GDJ.

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: GDJ)

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.

K153358Standard ClampStandard BariatricsK930315THORACIC CLAMPS: SAROT, KANTOWITZ AND LAWRENCEThomasville Medical Assoc.K924223MAR-MED LIVER STRAPMar-Med Co.K922659GENERAL SURGERY CLAMP AND NEEDLE HOLDERMiltex Instrument Co.K914913GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYSTIdeal Medical, Inc.K900956GS-7100 CHOLANGIOGRAM CLAMP, 5MMSolos Endoscopy, 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.

↑