FDA 510(k)

CONTROL-TIP CYSTOSCOPIC ELECTRODES

K-Number: K903156 · 1990-12-18

ApplicantNorth American Sterilization & Packaging Co.

Decision Date1990-12-18

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CONTROL-TIP CYSTOSCOPIC ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is North American Sterilization & Packaging Co.. It received FDA 510(k) clearance on 1990-12-18 under 510(k) number K903156. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROL-TIP CYSTOSCOPIC ELECTRODES?

CONTROL-TIP CYSTOSCOPIC ELECTRODES is a medical device that received FDA 510(k) clearance on 1990-12-18. The listed applicant is North American Sterilization & Packaging Co.. The 510(k) number is K903156.

When did CONTROL-TIP CYSTOSCOPIC ELECTRODES receive FDA 510(k) clearance?

CONTROL-TIP CYSTOSCOPIC ELECTRODES received FDA 510(k) clearance on 1990-12-18, under 510(k) number K903156.

Who is the listed applicant for CONTROL-TIP CYSTOSCOPIC ELECTRODES?

The FDA 510(k) record lists North American Sterilization & Packaging Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTROL-TIP CYSTOSCOPIC ELECTRODES?

The FDA product code for CONTROL-TIP CYSTOSCOPIC ELECTRODES is FAS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.