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FDA 510(k)

GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE

K-Number: K933174 · 1994-04-01

ApplicantGreenwald Surgical Co., Inc.
Decision Date1994-04-01
Product CodeFAS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GREENWALD FLEXIBLE ENDOSCOPIC 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 K933174. 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 FLEXIBLE ENDOSCOPIC ELECTRODE?

GREENWALD FLEXIBLE ENDOSCOPIC 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 K933174.

When did GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE receive FDA 510(k) clearance?

GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE received FDA 510(k) clearance on 1994-04-01, under 510(k) number K933174.

Who is the listed applicant for GREENWALD FLEXIBLE ENDOSCOPIC 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 FLEXIBLE ENDOSCOPIC ELECTRODE?

The FDA product code for GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE is FAS.

Related Clinical Trials

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Other records listing Greenwald Surgical Co., Inc. 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.

K933175GREENWALD CONTROL TIP URETEROSCOPIC ELECTRODEK933173GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODEK780137CLAMP, INCONTINENCE, BAUMRUCKER

Related Devices (Code: FAS)

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.

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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.

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