CLARIFIER-RICHARD-ALLAN
K-Number: K830627 · 1983-03-24
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Device Summary
Frequently Asked Questions
What is the CLARIFIER-RICHARD-ALLAN?
CLARIFIER-RICHARD-ALLAN is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K830627.
When did CLARIFIER-RICHARD-ALLAN receive FDA 510(k) clearance?
CLARIFIER-RICHARD-ALLAN received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830627.
Who is the listed applicant for CLARIFIER-RICHARD-ALLAN?
The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLARIFIER-RICHARD-ALLAN?
The FDA product code for CLARIFIER-RICHARD-ALLAN is KEM.
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 Richard-Allan Medical Ind., 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: KEM)
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.
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