MALIBU BATHING SYSTEM
K-Number: K925195 · 1994-10-17
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Device Summary
Frequently Asked Questions
What is the MALIBU BATHING SYSTEM?
MALIBU BATHING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-10-17. The listed applicant is Medi-Man Rehabilitation Products, Inc.. The 510(k) number is K925195.
When did MALIBU BATHING SYSTEM receive FDA 510(k) clearance?
MALIBU BATHING SYSTEM received FDA 510(k) clearance on 1994-10-17, under 510(k) number K925195.
Who is the listed applicant for MALIBU BATHING SYSTEM?
The FDA 510(k) record lists Medi-Man Rehabilitation Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MALIBU BATHING SYSTEM?
The FDA product code for MALIBU BATHING SYSTEM 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.
Other records listing Medi-Man Rehabilitation Products, 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: 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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