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FDA 510(k)

NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON

K-Number: K921646 · 1992-05-13

ApplicantNextec Corp.
Decision Date1992-05-13
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON is the device name listed in this FDA 510(k) record. The listed applicant is Nextec Corp.. It received FDA 510(k) clearance on 1992-05-13 under 510(k) number K921646. 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 NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON?

NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON is a medical device that received FDA 510(k) clearance on 1992-05-13. The listed applicant is Nextec Corp.. The 510(k) number is K921646.

When did NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON receive FDA 510(k) clearance?

NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON received FDA 510(k) clearance on 1992-05-13, under 510(k) number K921646.

Who is the listed applicant for NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON?

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

What is the FDA product code for NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON?

The FDA product code for NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON 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.

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Other records listing Nextec Corp. 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.

K922462NEXTEC FIBEROPTIC CABLESK920167NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL

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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