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FDA 510(k)

OCIDE HOSPITAL CLEANER-DISINFECTANT

K-Number: K945227 · 1995-03-23

Decision Date1995-03-23
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OCIDE HOSPITAL CLEANER-DISINFECTANT is the device name listed in this FDA 510(k) record. The listed applicant is Clariant Corporation. It received FDA 510(k) clearance on 1995-03-23 under 510(k) number K945227. 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 OCIDE HOSPITAL CLEANER-DISINFECTANT?

OCIDE HOSPITAL CLEANER-DISINFECTANT is a medical device that received FDA 510(k) clearance on 1995-03-23. The listed applicant is Clariant Corporation. The 510(k) number is K945227.

When did OCIDE HOSPITAL CLEANER-DISINFECTANT receive FDA 510(k) clearance?

OCIDE HOSPITAL CLEANER-DISINFECTANT received FDA 510(k) clearance on 1995-03-23, under 510(k) number K945227.

Who is the listed applicant for OCIDE HOSPITAL CLEANER-DISINFECTANT?

The FDA 510(k) record lists Clariant Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OCIDE HOSPITAL CLEANER-DISINFECTANT?

The FDA product code for OCIDE HOSPITAL CLEANER-DISINFECTANT 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 Clariant Corporation 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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