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FDA 510(k)

AMICON DIAFILTER 40. HEMOFILTER

K-Number: K840449 · 1984-03-23

ApplicantMedical Device Consultants, Inc.
Decision Date1984-03-23
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMICON DIAFILTER 40. HEMOFILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Consultants, Inc.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840449. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMICON DIAFILTER 40. HEMOFILTER?

AMICON DIAFILTER 40. HEMOFILTER is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Medical Device Consultants, Inc.. The 510(k) number is K840449.

When did AMICON DIAFILTER 40. HEMOFILTER receive FDA 510(k) clearance?

AMICON DIAFILTER 40. HEMOFILTER received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840449.

Who is the listed applicant for AMICON DIAFILTER 40. HEMOFILTER?

The FDA 510(k) record lists Medical Device Consultants, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMICON DIAFILTER 40. HEMOFILTER?

The FDA product code for AMICON DIAFILTER 40. HEMOFILTER is KDI.

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Related Devices (Code: KDI)

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.

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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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