UROLOGICAL LOOP RETRIEVERS
K-Number: K891252 · 1989-03-22
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Device Summary
Frequently Asked Questions
What is the UROLOGICAL LOOP RETRIEVERS?
UROLOGICAL LOOP RETRIEVERS is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Northgate Research, Inc.. The 510(k) number is K891252.
When did UROLOGICAL LOOP RETRIEVERS receive FDA 510(k) clearance?
UROLOGICAL LOOP RETRIEVERS received FDA 510(k) clearance on 1989-03-22, under 510(k) number K891252.
Who is the listed applicant for UROLOGICAL LOOP RETRIEVERS?
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 UROLOGICAL LOOP RETRIEVERS?
The FDA product code for UROLOGICAL LOOP RETRIEVERS is FGO.
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: FGO)
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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