RATTAN IMACS BY RATTAN INFORMATION CORPORATION
K-Number: K032176 · 2003-09-25
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Device Summary
Frequently Asked Questions
What is the RATTAN IMACS BY RATTAN INFORMATION CORPORATION?
RATTAN IMACS BY RATTAN INFORMATION CORPORATION is a medical device that received FDA 510(k) clearance on 2003-09-25. The listed applicant is Rattan Information Corporation. The 510(k) number is K032176.
When did RATTAN IMACS BY RATTAN INFORMATION CORPORATION receive FDA 510(k) clearance?
RATTAN IMACS BY RATTAN INFORMATION CORPORATION received FDA 510(k) clearance on 2003-09-25, under 510(k) number K032176.
Who is the listed applicant for RATTAN IMACS BY RATTAN INFORMATION CORPORATION?
The FDA 510(k) record lists Rattan Information Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RATTAN IMACS BY RATTAN INFORMATION CORPORATION?
The FDA product code for RATTAN IMACS BY RATTAN INFORMATION CORPORATION is LLZ.
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.
Related Devices (Code: LLZ)
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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