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FDA 510(k)

FIBER OPTIC LIGHT CABLE

K-Number: K903800 · 1990-08-29

ApplicantOrlux Engineering and Instrumentation
Decision Date1990-08-29
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC LIGHT CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Orlux Engineering and Instrumentation. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K903800. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC LIGHT CABLE?

FIBER OPTIC LIGHT CABLE is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Orlux Engineering and Instrumentation. The 510(k) number is K903800.

When did FIBER OPTIC LIGHT CABLE receive FDA 510(k) clearance?

FIBER OPTIC LIGHT CABLE received FDA 510(k) clearance on 1990-08-29, under 510(k) number K903800.

Who is the listed applicant for FIBER OPTIC LIGHT CABLE?

The FDA 510(k) record lists Orlux Engineering and Instrumentation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBER OPTIC LIGHT CABLE?

The FDA product code for FIBER OPTIC LIGHT CABLE is FST.

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 Orlux Engineering and Instrumentation 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.

K903790ENDOSCOPIC LIGHT SOURCE 250 ENDO

Related Devices (Code: FST)

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.

K200874TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal EndInnovasis, Inc.K122637LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999Stryker SpineK113697EIGR SURGICAL ILLUMINATION SYSTEMInvuity, Inc.K113330CABLECAPSensormedK102266ISOLED AC-POWERED LED HEADLIGHT SYSTEMIsolux, LLCK101496CABLECAP MODEL: WLF, STZ, ACMSensormed

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.

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