S-100 ALLEN-BROWN SHUNT
K-Number: K892663 · 1989-05-04
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Device Summary
Frequently Asked Questions
What is the S-100 ALLEN-BROWN SHUNT?
S-100 ALLEN-BROWN SHUNT is a medical device that received FDA 510(k) clearance on 1989-05-04. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K892663.
When did S-100 ALLEN-BROWN SHUNT receive FDA 510(k) clearance?
S-100 ALLEN-BROWN SHUNT received FDA 510(k) clearance on 1989-05-04, under 510(k) number K892663.
Who is the listed applicant for S-100 ALLEN-BROWN SHUNT?
The FDA 510(k) record lists Akcess Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S-100 ALLEN-BROWN SHUNT?
The FDA product code for S-100 ALLEN-BROWN SHUNT is FIQ.
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 Akcess Medical Products, 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: FIQ)
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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