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FDA 510(k)

PRECISE HOSPITAL FOAM CLEANER DISINFECTANT

K-Number: K951512 · 1995-08-07

Decision Date1995-08-07
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRECISE HOSPITAL FOAM CLEANER DISINFECTANT 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 1995-08-07 under 510(k) number K951512. 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 PRECISE HOSPITAL FOAM CLEANER DISINFECTANT?

PRECISE HOSPITAL FOAM CLEANER DISINFECTANT is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Caltech Industries, Inc.. The 510(k) number is K951512.

When did PRECISE HOSPITAL FOAM CLEANER DISINFECTANT receive FDA 510(k) clearance?

PRECISE HOSPITAL FOAM CLEANER DISINFECTANT received FDA 510(k) clearance on 1995-08-07, under 510(k) number K951512.

Who is the listed applicant for PRECISE HOSPITAL FOAM CLEANER DISINFECTANT?

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 PRECISE HOSPITAL FOAM CLEANER DISINFECTANT?

The FDA product code for PRECISE HOSPITAL FOAM 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 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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