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)

UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE

K-Number: K837278 · 1983-04-21

ApplicantUnterwasser-Electric GmbH
Decision Date1983-04-21
Product Code
DecisionSubstantially Equivalent

Device Summary

UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE is the device name listed in this FDA 510(k) record. The listed applicant is Unterwasser-Electric GmbH. It received FDA 510(k) clearance on 1983-04-21 under 510(k) number K837278. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE?

UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE is a medical device that received FDA 510(k) clearance on 1983-04-21. The listed applicant is Unterwasser-Electric GmbH. The 510(k) number is K837278.

When did UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE receive FDA 510(k) clearance?

UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE received FDA 510(k) clearance on 1983-04-21, under 510(k) number K837278.

Who is the listed applicant for UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE?

The FDA 510(k) record lists Unterwasser-Electric GmbH 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

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.

↑