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FDA 510(k)

HYDRAJUST IV UROLOGICAL TABLE

K-Number: K920742 · 1992-04-27

Decision Date1992-04-27
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HYDRAJUST IV UROLOGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1992-04-27 under 510(k) number K920742. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRAJUST IV UROLOGICAL TABLE?

HYDRAJUST IV UROLOGICAL TABLE is a medical device that received FDA 510(k) clearance on 1992-04-27. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K920742.

When did HYDRAJUST IV UROLOGICAL TABLE receive FDA 510(k) clearance?

HYDRAJUST IV UROLOGICAL TABLE received FDA 510(k) clearance on 1992-04-27, under 510(k) number K920742.

Who is the listed applicant for HYDRAJUST IV 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 IV UROLOGICAL TABLE?

The FDA product code for HYDRAJUST IV UROLOGICAL TABLE is IXR.

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.

View all 27 devices →

Related Devices (Code: IXR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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