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)

SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING

K-Number: K871400 · 1987-07-24

ApplicantGe Medical Systems Information Technologies
Decision Date1987-07-24
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1987-07-24 under 510(k) number K871400. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING?

SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING is a medical device that received FDA 510(k) clearance on 1987-07-24. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K871400.

When did SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING receive FDA 510(k) clearance?

SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING received FDA 510(k) clearance on 1987-07-24, under 510(k) number K871400.

Who is the listed applicant for SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING?

The FDA product code for SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING is DXK.

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 Ge Medical Systems Information Technologies 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.

K120770QT GUARD PLUS ANALYSIS SYSTEMK102426CARESCAPE MODEL V100 VITAL SIGNS MONITORK09236912SL ECG ANALYSIS PROGRAMK093141MARS HOLTER ANALYSIS WORKSTATIONK092027CARESCAPE MONITOR B850K090702MODIFICATION TO DASH 2500 PATIENT MONITOR

View all 136 devices →

Related Devices (Code: DXK)

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.

K181042Ultra ICE Plus – PI 9 MHz Peripheral Imaging CatheterBoston Scientific CorporationK160173Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter(eDFU), Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter (Paper DFU)Boston Scientific CorporationK031148IN-VISION IMAGING SYSTEMJomed, Inc.K9348879750 ATHENA ETHERNET OPTIONS & W Medico Teknik A/SK913209ACCESSORY TO GENESIS III (GCFM)Biosound, Inc.K911384CATHSCANNER(R) VISIONS(TM) 3.5F 54700/5.0F 54600Endosonics 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.

↑