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FDA 510(k)

PHENO-CEN SPRAY DISINFECTANT DEODORANT

K-Number: K951317 · 1995-04-25

Decision Date1995-04-25
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHENO-CEN SPRAY DISINFECTANT DEODORANT is the device name listed in this FDA 510(k) record. The listed applicant is Central Solutions, Inc.. It received FDA 510(k) clearance on 1995-04-25 under 510(k) number K951317. 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 PHENO-CEN SPRAY DISINFECTANT DEODORANT?

PHENO-CEN SPRAY DISINFECTANT DEODORANT is a medical device that received FDA 510(k) clearance on 1995-04-25. The listed applicant is Central Solutions, Inc.. The 510(k) number is K951317.

When did PHENO-CEN SPRAY DISINFECTANT DEODORANT receive FDA 510(k) clearance?

PHENO-CEN SPRAY DISINFECTANT DEODORANT received FDA 510(k) clearance on 1995-04-25, under 510(k) number K951317.

Who is the listed applicant for PHENO-CEN SPRAY DISINFECTANT DEODORANT?

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

What is the FDA product code for PHENO-CEN SPRAY DISINFECTANT DEODORANT?

The FDA product code for PHENO-CEN SPRAY DISINFECTANT DEODORANT 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 Central Solutions, 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 7 devices →

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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