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FDA 510(k)

INTRAORAL VIDEO SCOPE AND WINDOW TUBE

K-Number: K951019 · 1995-05-10

ApplicantCuda Products Co.
Decision Date1995-05-10
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTRAORAL VIDEO SCOPE AND WINDOW TUBE 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 1995-05-10 under 510(k) number K951019. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAORAL VIDEO SCOPE AND WINDOW TUBE?

INTRAORAL VIDEO SCOPE AND WINDOW TUBE is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Cuda Products Co.. The 510(k) number is K951019.

When did INTRAORAL VIDEO SCOPE AND WINDOW TUBE receive FDA 510(k) clearance?

INTRAORAL VIDEO SCOPE AND WINDOW TUBE received FDA 510(k) clearance on 1995-05-10, under 510(k) number K951019.

Who is the listed applicant for INTRAORAL VIDEO SCOPE AND WINDOW TUBE?

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 INTRAORAL VIDEO SCOPE AND WINDOW TUBE?

The FDA product code for INTRAORAL VIDEO SCOPE AND WINDOW TUBE is EIA.

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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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