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FDA 510(k)

CUDA SURGICAL LIGHT

K-Number: K901491 · 1990-06-18

ApplicantCuda Products Co.
Decision Date1990-06-18
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUDA SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Cuda Products Co.. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K901491. 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 CUDA SURGICAL LIGHT?

CUDA SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Cuda Products Co.. The 510(k) number is K901491.

When did CUDA SURGICAL LIGHT receive FDA 510(k) clearance?

CUDA SURGICAL LIGHT received FDA 510(k) clearance on 1990-06-18, under 510(k) number K901491.

Who is the listed applicant for CUDA SURGICAL LIGHT?

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

What is the FDA product code for CUDA SURGICAL LIGHT?

The FDA product code for CUDA SURGICAL LIGHT is FST.

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Other records listing Cuda Products Co. 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.

K983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEK981469CERMAX300 LIGHTSOURCEK980350VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150K980166LIGHTSOURCE OR ILLUMINATORK961074LIGHTSOURCE OR ILLUMINATOR

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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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