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FDA 510(k)

CONTROL III DISINFECTANT GERMICIDE

K-Number: K944179 · 1995-03-22

Decision Date1995-03-22
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTROL III DISINFECTANT GERMICIDE is the device name listed in this FDA 510(k) record. The listed applicant is Maril Products, Inc.. It received FDA 510(k) clearance on 1995-03-22 under 510(k) number K944179. 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 CONTROL III DISINFECTANT GERMICIDE?

CONTROL III DISINFECTANT GERMICIDE is a medical device that received FDA 510(k) clearance on 1995-03-22. The listed applicant is Maril Products, Inc.. The 510(k) number is K944179.

When did CONTROL III DISINFECTANT GERMICIDE receive FDA 510(k) clearance?

CONTROL III DISINFECTANT GERMICIDE received FDA 510(k) clearance on 1995-03-22, under 510(k) number K944179.

Who is the listed applicant for CONTROL III DISINFECTANT GERMICIDE?

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

What is the FDA product code for CONTROL III DISINFECTANT GERMICIDE?

The FDA product code for CONTROL III DISINFECTANT GERMICIDE 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 Maril Products, 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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