FDA 510(k)

CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE

K-Number: K800822 · 1980-06-17

ApplicantKli

Decision Date1980-06-17

Product CodeFAP

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K800822. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE?

CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Kli. The 510(k) number is K800822.

When did CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE receive FDA 510(k) clearance?

CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE received FDA 510(k) clearance on 1980-06-17, under 510(k) number K800822.

Who is the listed applicant for CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE?

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

What is the FDA product code for CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE?

The FDA product code for CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE is FAP.

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Other records listing Kli as applicant

K800913GYNECOLOGICAL CYSTO/URETHROSCOPE K781913INSUFFALATOR LAPARAOSCOPIC K781109FORCEPS, ELECTROSURGICAL K781089ONE INCISION BI-POLAR ELECTRO. FORCEPS K780955SCISSORS, HOOK, ELECTROSURGICAL K780954SCISSORS, HOOK, ELECTROSURGICAL

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Related Devices (Code: FAP)

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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.