1.9 FRENCH LITHOTRIPTER ELECTRODE
K-Number: K903337 · 1990-11-16
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Device Summary
Frequently Asked Questions
What is the 1.9 FRENCH LITHOTRIPTER ELECTRODE?
1.9 FRENCH LITHOTRIPTER ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-11-16. The listed applicant is Northgate Research, Inc.. The 510(k) number is K903337.
When did 1.9 FRENCH LITHOTRIPTER ELECTRODE receive FDA 510(k) clearance?
1.9 FRENCH LITHOTRIPTER ELECTRODE received FDA 510(k) clearance on 1990-11-16, under 510(k) number K903337.
Who is the listed applicant for 1.9 FRENCH LITHOTRIPTER 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 1.9 FRENCH LITHOTRIPTER ELECTRODE?
The FDA product code for 1.9 FRENCH LITHOTRIPTER 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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