ULTRAFREE-CL
K-Number: K941326 · 1994-05-27
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Device Summary
Frequently Asked Questions
What is the ULTRAFREE-CL?
ULTRAFREE-CL is a medical device that received FDA 510(k) clearance on 1994-05-27. The listed applicant is Millipore Corp.. The 510(k) number is K941326.
When did ULTRAFREE-CL receive FDA 510(k) clearance?
ULTRAFREE-CL received FDA 510(k) clearance on 1994-05-27, under 510(k) number K941326.
Who is the listed applicant for ULTRAFREE-CL?
The FDA 510(k) record lists Millipore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRAFREE-CL?
The FDA product code for ULTRAFREE-CL is JJH.
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 Millipore Corp. 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: JJH)
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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