CLYDE (TM) FILTRATION SYSTEM
K-Number: K864113 · 1987-02-04
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Device Summary
Frequently Asked Questions
What is the CLYDE (TM) FILTRATION SYSTEM?
CLYDE (TM) FILTRATION SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K864113.
When did CLYDE (TM) FILTRATION SYSTEM receive FDA 510(k) clearance?
CLYDE (TM) FILTRATION SYSTEM received FDA 510(k) clearance on 1987-02-04, under 510(k) number K864113.
Who is the listed applicant for CLYDE (TM) FILTRATION SYSTEM?
The FDA 510(k) record lists Arbor Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLYDE (TM) FILTRATION SYSTEM?
The FDA product code for CLYDE (TM) FILTRATION SYSTEM is FPB.
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 Arbor 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: FPB)
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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