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)

BEGOPAL

K-Number: K983078 · 1998-10-23

ApplicantBego U.S.A.
Decision Date1998-10-23
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEGOPAL is the device name listed in this FDA 510(k) record. The listed applicant is Bego U.S.A.. It received FDA 510(k) clearance on 1998-10-23 under 510(k) number K983078. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEGOPAL?

BEGOPAL is a medical device that received FDA 510(k) clearance on 1998-10-23. The listed applicant is Bego U.S.A.. The 510(k) number is K983078.

When did BEGOPAL receive FDA 510(k) clearance?

BEGOPAL received FDA 510(k) clearance on 1998-10-23, under 510(k) number K983078.

Who is the listed applicant for BEGOPAL?

The FDA 510(k) record lists Bego U.S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEGOPAL?

The FDA product code for BEGOPAL is EJS.

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 Bego U.S.A. 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.

K033279GOLD DENTAL CASTING ALLOYSK032136WIROBOND CK983080AUROLLOYD KFK983082BEGOCER GK983077BIO PONTOSTARK983079PLATINLLOYD 100

View all 7 devices →

Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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.

↑