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)

HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT

K-Number: K930265 · 1995-04-25

ApplicantGE Medical Systems
Decision Date1995-04-25
Product CodeLNI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1995-04-25 under 510(k) number K930265. The device is classified under product code LNI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT?

HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT is a medical device that received FDA 510(k) clearance on 1995-04-25. The listed applicant is GE Medical Systems. The 510(k) number is K930265.

When did HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT receive FDA 510(k) clearance?

HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT received FDA 510(k) clearance on 1995-04-25, under 510(k) number K930265.

Who is the listed applicant for HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT?

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

What is the FDA product code for HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT?

The FDA product code for HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT is LNI.

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 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.

K253808AIR Recon DLK220848Venue FitK220851VenueK173341Vivid E80, Vivid E90, Vivid E95K103411IDEAL IQ SOFTWARE OPTIONK073138CARDIQ EXPRESS VERSION 2.0

View all 170 devices →

Related Devices (Code: LNI)

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.

K093044OASIS MRI SYSTEMHitachi Medical Systems America, Inc.K071506ECHELON SPECTROSCOPY PACKAGEHitachi Medical Systems America, Inc.K011604PROSTATE SPECTROSCOPY AND IMAGING EXAM (PROSE) SOFTWARE OPTION FOR MRIGe Medical Systems, Inc.K010129EXCELART WITH PIANISSIMO, MODEL MRT-1500/P3Toshiba America Medical Systems, In.CK003575MODIFICATION TO 3.0T SIGNA VH/I MAGNETIC RESONANCE SYSTEMGE Medical SystemsK991568MR SPECTROSCOPY PACKAGEPhilips Medical Systems (Cleveland), 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.

↑