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FDA 510(k)

FIAGEN FERRITIN

K-Number: K882822 · 1988-08-04

ApplicantCyberfluor, Inc.
Decision Date1988-08-04
Product CodeDFL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

FIAGEN FERRITIN is the device name listed in this FDA 510(k) record. The listed applicant is Cyberfluor, Inc.. It received FDA 510(k) clearance on 1988-08-04 under 510(k) number K882822. The device is classified under product code DFL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIAGEN FERRITIN?

FIAGEN FERRITIN is a medical device that received FDA 510(k) clearance on 1988-08-04. The listed applicant is Cyberfluor, Inc.. The 510(k) number is K882822.

When did FIAGEN FERRITIN receive FDA 510(k) clearance?

FIAGEN FERRITIN received FDA 510(k) clearance on 1988-08-04, under 510(k) number K882822.

Who is the listed applicant for FIAGEN FERRITIN?

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

What is the FDA product code for FIAGEN FERRITIN?

The FDA product code for FIAGEN FERRITIN is DFL.

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Other records listing Cyberfluor, 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.

K923410FIAGEN PROGESTERONEK905656FLAGEN TRIIODOTHYRONINE (T3) ASSAYK904539FLAGEN TM FREE T4K900621FIAGEN(TM) HLH.SK895186FIAGEN T3 UPTAKE CATALOGUE #101-402K895396CYBERFLUOR FIAGEN TSH

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Related Devices (Code: DFL)

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.

K883493TECHNICON DPA-1 IMMUNOGLOBULIN MTechnicon Instruments Corp.K772079RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.MGelman Instrument Co.

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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