EVACUATOR, GASTRO-UROLOGY
K-Number: K921451 · 1992-10-28
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Device Summary
Frequently Asked Questions
What is the EVACUATOR, GASTRO-UROLOGY?
EVACUATOR, GASTRO-UROLOGY is a medical device that received FDA 510(k) clearance on 1992-10-28. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K921451.
When did EVACUATOR, GASTRO-UROLOGY receive FDA 510(k) clearance?
EVACUATOR, GASTRO-UROLOGY received FDA 510(k) clearance on 1992-10-28, under 510(k) number K921451.
Who is the listed applicant for EVACUATOR, GASTRO-UROLOGY?
The FDA 510(k) record lists Northgate Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVACUATOR, GASTRO-UROLOGY?
The FDA product code for EVACUATOR, GASTRO-UROLOGY is KQT.
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 Technologies, 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: KQT)
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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