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FDA 510(k)

CABLECAP MODEL: WLF, STZ, ACM

K-Number: K101496 · 2010-09-14

ApplicantSensormed
Decision Date2010-09-14
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CABLECAP MODEL: WLF, STZ, ACM is the device name listed in this FDA 510(k) record. The listed applicant is Sensormed. It received FDA 510(k) clearance on 2010-09-14 under 510(k) number K101496. 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 CABLECAP MODEL: WLF, STZ, ACM?

CABLECAP MODEL: WLF, STZ, ACM is a medical device that received FDA 510(k) clearance on 2010-09-14. The listed applicant is Sensormed. The 510(k) number is K101496.

When did CABLECAP MODEL: WLF, STZ, ACM receive FDA 510(k) clearance?

CABLECAP MODEL: WLF, STZ, ACM received FDA 510(k) clearance on 2010-09-14, under 510(k) number K101496.

Who is the listed applicant for CABLECAP MODEL: WLF, STZ, ACM?

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

What is the FDA product code for CABLECAP MODEL: WLF, STZ, ACM?

The FDA product code for CABLECAP MODEL: WLF, STZ, ACM 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 Sensormed 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.

K113330CABLECAP

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, LLCK10038821ST CENTURY CENTURION EXCELED AND SYSTEM TWO LED LIGHTING SYSTEMSMedical Illumination International, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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