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)

SIGHTFIX

K-Number: K024251 · 2003-03-18

ApplicantWorld of Medicine Lemke GmbH
Decision Date2003-03-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SIGHTFIX is the device name listed in this FDA 510(k) record. The listed applicant is World of Medicine Lemke GmbH. It received FDA 510(k) clearance on 2003-03-18 under 510(k) number K024251. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGHTFIX?

SIGHTFIX is a medical device that received FDA 510(k) clearance on 2003-03-18. The listed applicant is World of Medicine Lemke GmbH. The 510(k) number is K024251.

When did SIGHTFIX receive FDA 510(k) clearance?

SIGHTFIX received FDA 510(k) clearance on 2003-03-18, under 510(k) number K024251.

Who is the listed applicant for SIGHTFIX?

The FDA 510(k) record lists World of Medicine Lemke GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIGHTFIX?

The FDA product code for SIGHTFIX is GCJ.

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 World of Medicine Lemke GmbH 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.

K023468ENDOSCOPIC LIGHT SOURCE XL180/L3K021717ENDOSCOPIC LIGHT SOURCE, MODEL XL300/L5K021456ER150/M2K020889ENDOSCOPIC LIGHT SOURCE XL202/L3K014158ENDOSCOPIC CAMERA TC804/C4K020336ENDOSCOPIC CAMERA MC404/C3

View all 7 devices →

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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.

↑