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)

SERVOMED MEDIVISION SCOPE SMV-235

K-Number: K840209 · 1984-09-20

ApplicantLitton Medical Electronics
Decision Date1984-09-20
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERVOMED MEDIVISION SCOPE SMV-235 is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1984-09-20 under 510(k) number K840209. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVOMED MEDIVISION SCOPE SMV-235?

SERVOMED MEDIVISION SCOPE SMV-235 is a medical device that received FDA 510(k) clearance on 1984-09-20. The listed applicant is Litton Medical Electronics. The 510(k) number is K840209.

When did SERVOMED MEDIVISION SCOPE SMV-235 receive FDA 510(k) clearance?

SERVOMED MEDIVISION SCOPE SMV-235 received FDA 510(k) clearance on 1984-09-20, under 510(k) number K840209.

Who is the listed applicant for SERVOMED MEDIVISION SCOPE SMV-235?

The FDA 510(k) record lists Litton Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERVOMED MEDIVISION SCOPE SMV-235?

The FDA product code for SERVOMED MEDIVISION SCOPE SMV-235 is DXJ.

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 Litton Medical Electronics 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.

K840522RECOMED BLOOD-FLOW METER H236-052-02K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840439RECOMED CARDIAC OUTPUT METER 236067-K840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840832SERVOMED OXCARDIORE SPIROGRAPH 324/111

View all 38 devices →

Related Devices (Code: DXJ)

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.

K212003ESSENZ Patient MonitorLivanova Deutschland, GmbHK212208Philips IntelliVue GuardianSoftware (Rev. E.0X)Philips Medizin Systeme Boeblingen GmbHK201162Essence 55SP Large Monitor SystemShenyang Torch-Bigtide Digital Technology Co., Ltd.K173107Vios Central Station Monitor Software, Vios Central Server SoftwareVios Medical, Inc.K180534Philips IntelliVue GuardianSoftwarePhilips Medizin Systeme Boeblingen GmbHK173381Nexxis ORBarco N.V.

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.

↑