JACKSON HYDRO SYSTEM
K-Number: K802780 · 1980-12-10
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Device Summary
Frequently Asked Questions
What is the JACKSON HYDRO SYSTEM?
JACKSON HYDRO SYSTEM is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is S. Jackson, Inc.. The 510(k) number is K802780.
When did JACKSON HYDRO SYSTEM receive FDA 510(k) clearance?
JACKSON HYDRO SYSTEM received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802780.
Who is the listed applicant for JACKSON HYDRO SYSTEM?
The FDA 510(k) record lists S. Jackson, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JACKSON HYDRO SYSTEM?
The FDA product code for JACKSON HYDRO SYSTEM is FNG.
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 S. Jackson, 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: FNG)
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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