PARKER BATHING SYSTEM
K-Number: K883308 · 1988-09-22
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Device Summary
Frequently Asked Questions
What is the PARKER BATHING SYSTEM?
PARKER BATHING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-22. The listed applicant is Mid-Canada Medical. The 510(k) number is K883308.
When did PARKER BATHING SYSTEM receive FDA 510(k) clearance?
PARKER BATHING SYSTEM received FDA 510(k) clearance on 1988-09-22, under 510(k) number K883308.
Who is the listed applicant for PARKER BATHING SYSTEM?
The FDA 510(k) record lists Mid-Canada Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARKER BATHING SYSTEM?
The FDA product code for PARKER 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 Mid-Canada Medical 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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