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FDA 510(k)

MINICON CONCENTRATOR

K-Number: K760592 · 1976-11-23

ApplicantAmicon, Inc.
Decision Date1976-11-23
Product CodeJJH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINICON 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 1976-11-23 under 510(k) number K760592. 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 MINICON CONCENTRATOR?

MINICON CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1976-11-23. The listed applicant is Amicon, Inc.. The 510(k) number is K760592.

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

MINICON CONCENTRATOR received FDA 510(k) clearance on 1976-11-23, under 510(k) number K760592.

Who is the listed applicant for MINICON 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 MINICON CONCENTRATOR?

The FDA product code for MINICON 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 HEMOFILTERK893733CENTRICON CONCENTRATOR

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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.K943965VIVAPORE 10Vivascience, Inc.K943966VIVAPORE 2Vivascience, 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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