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)

SHARED VISION(PART NUMBER SV 0015)

K-Number: K961753 · 1996-07-25

ApplicantImagelabs, Inc.
Decision Date1996-07-25
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHARED VISION(PART NUMBER SV 0015) is the device name listed in this FDA 510(k) record. The listed applicant is Imagelabs, Inc.. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K961753. 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 SHARED VISION(PART NUMBER SV 0015)?

SHARED VISION(PART NUMBER SV 0015) is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Imagelabs, Inc.. The 510(k) number is K961753.

When did SHARED VISION(PART NUMBER SV 0015) receive FDA 510(k) clearance?

SHARED VISION(PART NUMBER SV 0015) received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961753.

Who is the listed applicant for SHARED VISION(PART NUMBER SV 0015)?

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

What is the FDA product code for SHARED VISION(PART NUMBER SV 0015)?

The FDA product code for SHARED VISION(PART NUMBER SV 0015) 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

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.

↑