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FDA 510(k)

VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150

K-Number: K980350 · 1998-04-28

ApplicantCuda Products Co.
Decision Date1998-04-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150 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 1998-04-28 under 510(k) number K980350. 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 VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150?

VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150 is a medical device that received FDA 510(k) clearance on 1998-04-28. The listed applicant is Cuda Products Co.. The 510(k) number is K980350.

When did VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150 receive FDA 510(k) clearance?

VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150 received FDA 510(k) clearance on 1998-04-28, under 510(k) number K980350.

Who is the listed applicant for VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150?

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 VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150?

The FDA product code for VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150 is GCJ.

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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 LIGHTSOURCEK980166LIGHTSOURCE OR ILLUMINATORK961074LIGHTSOURCE OR ILLUMINATORK951019INTRAORAL VIDEO SCOPE AND WINDOW TUBE

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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.

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