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)

LINX NETWORKING SYSTEM

K-Number: K964250 · 1996-12-18

ApplicantSterling Diagnostic Imaging, Inc.
Decision Date1996-12-18
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINX NETWORKING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Diagnostic Imaging, Inc.. It received FDA 510(k) clearance on 1996-12-18 under 510(k) number K964250. 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 LINX NETWORKING SYSTEM?

LINX NETWORKING SYSTEM is a medical device that received FDA 510(k) clearance on 1996-12-18. The listed applicant is Sterling Diagnostic Imaging, Inc.. The 510(k) number is K964250.

When did LINX NETWORKING SYSTEM receive FDA 510(k) clearance?

LINX NETWORKING SYSTEM received FDA 510(k) clearance on 1996-12-18, under 510(k) number K964250.

Who is the listed applicant for LINX NETWORKING SYSTEM?

The FDA 510(k) record lists Sterling Diagnostic Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINX NETWORKING SYSTEM?

The FDA product code for LINX NETWORKING 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 Sterling Diagnostic Imaging, Inc. 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.

K980970IIRAD DIRECTRAY OPERATOR CONSOLEK980220IISYS PACS SYSTEMK974423ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAILK973206STERLING DIAGNOSTIC IMAGING DIRECT RADIOGRAPHYK972660RAVEN DRY PRINTERK973028HELIOS LASER IMAGER 1417

View all 7 devices →

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.K992426RAYPAX WEB CLINICAL SYSTEMSamsung Sds Co., Ltd.K992352ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0Inteleradiology, Inc.K991537SAMSUNG RAYPAX SYSTEMSamsung Sds Co., Ltd.K984000STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEMSurgical Navigation Technologies, 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.

↑