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)

CLARIFIER-RICHARD-ALLAN

K-Number: K830627 · 1983-03-24

Decision Date1983-03-24
Product CodeKEM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CLARIFIER-RICHARD-ALLAN is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830627. The device is classified under product code KEM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 33 devices →

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.

↑