HYDRAJUST III UROLOGICAL TABLE
K-Number: K860040 · 1986-02-10
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Device Summary
Frequently Asked Questions
What is the HYDRAJUST III UROLOGICAL TABLE?
HYDRAJUST III UROLOGICAL TABLE is a medical device that received FDA 510(k) clearance on 1986-02-10. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K860040.
When did HYDRAJUST III UROLOGICAL TABLE receive FDA 510(k) clearance?
HYDRAJUST III UROLOGICAL TABLE received FDA 510(k) clearance on 1986-02-10, under 510(k) number K860040.
Who is the listed applicant for HYDRAJUST III UROLOGICAL TABLE?
The FDA 510(k) record lists Mallinckrodt Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYDRAJUST III UROLOGICAL TABLE?
The FDA product code for HYDRAJUST III UROLOGICAL TABLE is KQS.
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 Mallinckrodt Group, 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: KQS)
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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