SYRINGEFILTER
K-Number: K960928 · 1997-04-04
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Device Summary
Frequently Asked Questions
What is the SYRINGEFILTER?
SYRINGEFILTER is a medical device that received FDA 510(k) clearance on 1997-04-04. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K960928.
When did SYRINGEFILTER receive FDA 510(k) clearance?
SYRINGEFILTER received FDA 510(k) clearance on 1997-04-04, under 510(k) number K960928.
Who is the listed applicant for SYRINGEFILTER?
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 SYRINGEFILTER?
The FDA product code for SYRINGEFILTER is BSN.
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: BSN)
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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