GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09
K-Number: K002596 · 2001-02-15
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Device Summary
Frequently Asked Questions
What is the GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09?
GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09 is a medical device that received FDA 510(k) clearance on 2001-02-15. The listed applicant is Gebauer Co.. The 510(k) number is K002596.
When did GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09 receive FDA 510(k) clearance?
GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09 received FDA 510(k) clearance on 2001-02-15, under 510(k) number K002596.
Who is the listed applicant for GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09?
The FDA 510(k) record lists Gebauer Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09?
The FDA product code for GEBAUER'S FLURO ETHYL, MODEL 0386-0002-09 is MLY.
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 Gebauer Co. 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: MLY)
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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