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FDA 510(k)

CENTRIPREP 100

K-Number: K900280 · 1990-02-16

ApplicantAmicon, Inc.
Decision Date1990-02-16
Product CodeJJP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIPREP 100 is the device name listed in this FDA 510(k) record. The listed applicant is Amicon, Inc.. It received FDA 510(k) clearance on 1990-02-16 under 510(k) number K900280. The device is classified under product code JJP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIPREP 100?

CENTRIPREP 100 is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Amicon, Inc.. The 510(k) number is K900280.

When did CENTRIPREP 100 receive FDA 510(k) clearance?

CENTRIPREP 100 received FDA 510(k) clearance on 1990-02-16, under 510(k) number K900280.

Who is the listed applicant for CENTRIPREP 100?

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 CENTRIPREP 100?

The FDA product code for CENTRIPREP 100 is JJP.

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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 SETK895405AMICON MINIFILTER PLUS HEMOFILTERK893733CENTRICON CONCENTRATORK892645AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY

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Related Devices (Code: JJP)

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.

K863438NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZERNova Biomedical Corp.K860143URINE DILUENT-FOR USE WITH ION SELECTIVE ELECTRODEReagent Laboratory, Inc.

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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