AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS
K-Number: K922160 · 1992-06-19
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Device Summary
Frequently Asked Questions
What is the AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS?
AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS is a medical device that received FDA 510(k) clearance on 1992-06-19. The listed applicant is Aquamotion, Inc.. The 510(k) number is K922160.
When did AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS receive FDA 510(k) clearance?
AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS received FDA 510(k) clearance on 1992-06-19, under 510(k) number K922160.
Who is the listed applicant for AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS?
The FDA 510(k) record lists Aquamotion, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS?
The FDA product code for AQUAMOTION BY FERNO ILLE HYDROTHERAPY POOLS is ILJ.
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.
Related Devices (Code: ILJ)
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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