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FDA 510(k)

CENTRICON CONCENTRATOR

K-Number: K893733 · 1989-07-20

ApplicantAmicon, Inc.
Decision Date1989-07-20
Product CodeJJH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRICON CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Amicon, Inc.. It received FDA 510(k) clearance on 1989-07-20 under 510(k) number K893733. The device is classified under product code JJH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRICON CONCENTRATOR?

CENTRICON CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Amicon, Inc.. The 510(k) number is K893733.

When did CENTRICON CONCENTRATOR receive FDA 510(k) clearance?

CENTRICON CONCENTRATOR received FDA 510(k) clearance on 1989-07-20, under 510(k) number K893733.

Who is the listed applicant for CENTRICON 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 CONCENTRATOR?

The FDA product code for CENTRICON CONCENTRATOR is JJH.

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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.

K930168CENTRICON -50 CONCENTRATORK902837AMICON DIAFILTER 30 HEMOCONCENTRATORK901286AMICON HEMOCONCENTRATOR SETK900280CENTRIPREP 100K895405AMICON MINIFILTER PLUS HEMOFILTERK892645AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY

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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.

K113731ESENSOR RESPIRATORY VIRAL PANELClinical Micro Sensors, Inc.K960298VIVASPIN 4 10,000 MWVivascience, Inc.K943966VIVAPORE 2Vivascience, Inc.K943965VIVAPORE 10Vivascience, Inc.K941326ULTRAFREE-CLMillipore Corp.K935496NANOSEP N10Intersep , Ltd.

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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