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FDA 510(k)

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE

K-Number: K062399 · 2006-11-17

ApplicantRockwell Medical Technologies, Inc.
Decision Date2006-11-17
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE is the device name listed in this FDA 510(k) record. The listed applicant is Rockwell Medical Technologies, Inc.. It received FDA 510(k) clearance on 2006-11-17 under 510(k) number K062399. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE?

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE is a medical device that received FDA 510(k) clearance on 2006-11-17. The listed applicant is Rockwell Medical Technologies, Inc.. The 510(k) number is K062399.

When did ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE receive FDA 510(k) clearance?

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE received FDA 510(k) clearance on 2006-11-17, under 510(k) number K062399.

Who is the listed applicant for ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE?

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

What is the FDA product code for ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE?

The FDA product code for ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE is KPO.

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Other records listing Rockwell Medical Technologies, Inc. as applicant

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Related Devices (Code: KPO)

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.

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Official Source

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