CENTRICON MICRO-CONCENTRATOR
K-Number: K833919 · 1984-01-30
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Device Summary
Frequently Asked Questions
What is the CENTRICON MICRO-CONCENTRATOR?
CENTRICON MICRO-CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Amicon, Inc.. The 510(k) number is K833919.
When did CENTRICON MICRO-CONCENTRATOR receive FDA 510(k) clearance?
CENTRICON MICRO-CONCENTRATOR received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833919.
Who is the listed applicant for CENTRICON MICRO-CONCENTRATOR?
The FDA 510(k) record lists Amicon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRICON MICRO-CONCENTRATOR?
The FDA product code for CENTRICON MICRO-CONCENTRATOR 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 Amicon, 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: 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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