Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRI-CEN GERMICIDAL DETERGENT

K-Number: K951020 · 1995-08-28

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

Device Summary

TRI-CEN GERMICIDAL DETERGENT 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 1995-08-28 under 510(k) number K951020. 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 TRI-CEN GERMICIDAL DETERGENT?

TRI-CEN GERMICIDAL DETERGENT is a medical device that received FDA 510(k) clearance on 1995-08-28. The listed applicant is Central Solutions, Inc.. The 510(k) number is K951020.

When did TRI-CEN GERMICIDAL DETERGENT receive FDA 510(k) clearance?

TRI-CEN GERMICIDAL DETERGENT received FDA 510(k) clearance on 1995-08-28, under 510(k) number K951020.

Who is the listed applicant for TRI-CEN GERMICIDAL DETERGENT?

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 TRI-CEN GERMICIDAL DETERGENT?

The FDA product code for TRI-CEN GERMICIDAL DETERGENT 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑