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FDA 510(k)

CITRACE HOSPITAL GERMICIDAL DEODORIZER

K-Number: K952405 · 1995-08-28

Decision Date1995-08-28
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CITRACE HOSPITAL GERMICIDAL DEODORIZER is the device name listed in this FDA 510(k) record. The listed applicant is Caltech Industries, Inc.. It received FDA 510(k) clearance on 1995-08-28 under 510(k) number K952405. The device is classified under product code LRJ. It was reviewed by the HO advisory panel. Product code LRJ falls under the category of Clinical Lab, which includes general clinical laboratory instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CITRACE HOSPITAL GERMICIDAL DEODORIZER?

CITRACE HOSPITAL GERMICIDAL DEODORIZER is a medical device that received FDA 510(k) clearance on 1995-08-28. The listed applicant is Caltech Industries, Inc.. The 510(k) number is K952405.

When did CITRACE HOSPITAL GERMICIDAL DEODORIZER receive FDA 510(k) clearance?

CITRACE HOSPITAL GERMICIDAL DEODORIZER received FDA 510(k) clearance on 1995-08-28, under 510(k) number K952405.

Who is the listed applicant for CITRACE HOSPITAL GERMICIDAL DEODORIZER?

The FDA 510(k) record lists Caltech Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CITRACE HOSPITAL GERMICIDAL DEODORIZER?

The FDA product code for CITRACE HOSPITAL GERMICIDAL DEODORIZER is LRJ. This falls under the Clinical Lab category.

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 Caltech Industries, 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: LRJ)

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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