FDA 510(k)

GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE

K-Number: K933173 · 1994-04-01

Decision Date1994-04-01

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Greenwald Surgical Co., Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K933173. 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 GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE?

GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Greenwald Surgical Co., Inc.. The 510(k) number is K933173.

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

GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE received FDA 510(k) clearance on 1994-04-01, under 510(k) number K933173.

Who is the listed applicant for GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE?

The FDA 510(k) record lists Greenwald Surgical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Other records listing Greenwald Surgical Co., Inc. as applicant

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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.