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FDA 510(k)

RIA-GNOST FERRITIN

K-Number: K890697 · 1989-03-16

ApplicantCambridge Medical Technology
Decision Date1989-03-16
Product CodeJMG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RIA-GNOST FERRITIN is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Medical Technology. It received FDA 510(k) clearance on 1989-03-16 under 510(k) number K890697. The device is classified under product code JMG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA-GNOST FERRITIN?

RIA-GNOST FERRITIN is a medical device that received FDA 510(k) clearance on 1989-03-16. The listed applicant is Cambridge Medical Technology. The 510(k) number is K890697.

When did RIA-GNOST FERRITIN receive FDA 510(k) clearance?

RIA-GNOST FERRITIN received FDA 510(k) clearance on 1989-03-16, under 510(k) number K890697.

Who is the listed applicant for RIA-GNOST FERRITIN?

The FDA 510(k) record lists Cambridge Medical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA-GNOST FERRITIN?

The FDA product code for RIA-GNOST FERRITIN is JMG.

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Other records listing Cambridge Medical Technology 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.

K890837RIA-GNOST INSULINK890836RIA-GNOST PROGESTERONEK873737NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAYK870573T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KITK862871RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOLK860130TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KIT

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Related Devices (Code: JMG)

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.

K234052Access FerritinBeckman Coulter, Inc.K052082FERRITIN ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 33020Beckman Coulter, Inc.K964282TINA-QUANT FERRITIN ASSAYBoehringer Mannheim Corp.K971833ELECSYS FERRITINBoehringer Mannheim Corp.K963498FERR FLEX REAGENT CARTRIDGEDade Chemistry Systems, Inc.K950393ACE(TM) CEDIA(R) FERRITIN ASSAYSchiapparelli Biosystems, 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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