1500 EO EXHAUST HOOD
K-Number: K792660 · 1980-01-29
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Device Summary
Frequently Asked Questions
What is the 1500 EO EXHAUST HOOD?
1500 EO EXHAUST HOOD is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Castle Co.. The 510(k) number is K792660.
When did 1500 EO EXHAUST HOOD receive FDA 510(k) clearance?
1500 EO EXHAUST HOOD received FDA 510(k) clearance on 1980-01-29, under 510(k) number K792660.
Who is the listed applicant for 1500 EO EXHAUST HOOD?
The FDA 510(k) record lists Castle Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1500 EO EXHAUST HOOD?
The FDA product code for 1500 EO EXHAUST HOOD is FLF.
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 Castle 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: FLF)
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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