CEA-IMMERSIBLE SEPARATOR
K-Number: K781043 · 1978-09-15
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Device Summary
Frequently Asked Questions
What is the CEA-IMMERSIBLE SEPARATOR?
CEA-IMMERSIBLE SEPARATOR is a medical device that received FDA 510(k) clearance on 1978-09-15. The listed applicant is Millipore Corp.. The 510(k) number is K781043.
When did CEA-IMMERSIBLE SEPARATOR receive FDA 510(k) clearance?
CEA-IMMERSIBLE SEPARATOR received FDA 510(k) clearance on 1978-09-15, under 510(k) number K781043.
Who is the listed applicant for CEA-IMMERSIBLE SEPARATOR?
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 CEA-IMMERSIBLE SEPARATOR?
The FDA product code for CEA-IMMERSIBLE SEPARATOR is JRL.
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: JRL)
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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