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FDA 510(k)

2.5 FRENCH LITHOTRIPTOR ELECTRODE

K-Number: K894704 · 1989-10-18

Decision Date1989-10-18
Product CodeFFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

2.5 FRENCH LITHOTRIPTOR ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Research, Inc.. It received FDA 510(k) clearance on 1989-10-18 under 510(k) number K894704. The device is classified under product code FFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2.5 FRENCH LITHOTRIPTOR ELECTRODE?

2.5 FRENCH LITHOTRIPTOR ELECTRODE is a medical device that received FDA 510(k) clearance on 1989-10-18. The listed applicant is Northgate Research, Inc.. The 510(k) number is K894704.

When did 2.5 FRENCH LITHOTRIPTOR ELECTRODE receive FDA 510(k) clearance?

2.5 FRENCH LITHOTRIPTOR ELECTRODE received FDA 510(k) clearance on 1989-10-18, under 510(k) number K894704.

Who is the listed applicant for 2.5 FRENCH LITHOTRIPTOR ELECTRODE?

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

What is the FDA product code for 2.5 FRENCH LITHOTRIPTOR ELECTRODE?

The FDA product code for 2.5 FRENCH LITHOTRIPTOR ELECTRODE is FFK.

Related Clinical Trials

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.

Other records listing Northgate Research, 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.

View all 8 devices →

Related Devices (Code: FFK)

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.

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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