CSF AUTOMATED CONTROL, MODELS CSF001, CSF003
K-Number: K072846 · 2007-11-26
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Device Summary
Frequently Asked Questions
What is the CSF AUTOMATED CONTROL, MODELS CSF001, CSF003?
CSF AUTOMATED CONTROL, MODELS CSF001, CSF003 is a medical device that received FDA 510(k) clearance on 2007-11-26. The listed applicant is R&D Systems, Inc.. The 510(k) number is K072846.
When did CSF AUTOMATED CONTROL, MODELS CSF001, CSF003 receive FDA 510(k) clearance?
CSF AUTOMATED CONTROL, MODELS CSF001, CSF003 received FDA 510(k) clearance on 2007-11-26, under 510(k) number K072846.
Who is the listed applicant for CSF AUTOMATED CONTROL, MODELS CSF001, CSF003?
The FDA 510(k) record lists R&D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CSF AUTOMATED CONTROL, MODELS CSF001, CSF003?
The FDA product code for CSF AUTOMATED CONTROL, MODELS CSF001, CSF003 is JPK.
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 R&D Systems, 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: JPK)
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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