GISH ARTERIAL FILTER
K-Number: K914791 · 1993-04-06
Advertisement
Device Summary
Frequently Asked Questions
What is the GISH ARTERIAL FILTER?
GISH ARTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K914791.
When did GISH ARTERIAL FILTER receive FDA 510(k) clearance?
GISH ARTERIAL FILTER received FDA 510(k) clearance on 1993-04-06, under 510(k) number K914791.
Who is the listed applicant for GISH ARTERIAL FILTER?
The FDA 510(k) record lists Gish Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GISH ARTERIAL FILTER?
The FDA product code for GISH ARTERIAL FILTER is DTM.
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 Gish Biomedical, 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: DTM)
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.
Advertisement