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)

RAYPAX WEB CLINICAL SYSTEM

K-Number: K992426 · 1999-10-13

ApplicantSamsung Sds Co., Ltd.
Decision Date1999-10-13
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RAYPAX WEB CLINICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Samsung Sds Co., Ltd.. It received FDA 510(k) clearance on 1999-10-13 under 510(k) number K992426. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYPAX WEB CLINICAL SYSTEM?

RAYPAX WEB CLINICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1999-10-13. The listed applicant is Samsung Sds Co., Ltd.. The 510(k) number is K992426.

When did RAYPAX WEB CLINICAL SYSTEM receive FDA 510(k) clearance?

RAYPAX WEB CLINICAL SYSTEM received FDA 510(k) clearance on 1999-10-13, under 510(k) number K992426.

Who is the listed applicant for RAYPAX WEB CLINICAL SYSTEM?

The FDA 510(k) record lists Samsung Sds Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAYPAX WEB CLINICAL SYSTEM?

The FDA product code for RAYPAX WEB CLINICAL SYSTEM is LMD.

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 Samsung Sds Co., Ltd. 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.

K002062SAMSUNG 10DR IMPLANT SYSTEMK992306SAMSUNG RAYPAX DISPLAY WORKSTATIONK992131SAMSUNG RAYPAX LONG TERM ARCHIVEK992112SAMSUNG RAYPAX FILM DIGITIZERK991537SAMSUNG RAYPAX SYSTEM

Related Devices (Code: LMD)

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.

K994329IIVS INTEGRATED IMAGE VIEWING STATIONTerarecon,Inc.K992698STENTOR, PAGEVIEWStentor, Inc.K992352ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0Inteleradiology, Inc.K991537SAMSUNG RAYPAX SYSTEMSamsung Sds Co., Ltd.K984000STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEMSurgical Navigation Technologies, Inc.K974707IMAGEQUESTVisual Med, 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.

↑