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FDA 510(k)

EASYRA MG REAGENT, MODEL 10220

K-Number: K092737 · 2009-11-17

ApplicantMedica Corp.
Decision Date2009-11-17
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EASYRA MG REAGENT, MODEL 10220 is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 2009-11-17 under 510(k) number K092737. The device is classified under product code JGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYRA MG REAGENT, MODEL 10220?

EASYRA MG REAGENT, MODEL 10220 is a medical device that received FDA 510(k) clearance on 2009-11-17. The listed applicant is Medica Corp.. The 510(k) number is K092737.

When did EASYRA MG REAGENT, MODEL 10220 receive FDA 510(k) clearance?

EASYRA MG REAGENT, MODEL 10220 received FDA 510(k) clearance on 2009-11-17, under 510(k) number K092737.

Who is the listed applicant for EASYRA MG REAGENT, MODEL 10220?

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

What is the FDA product code for EASYRA MG REAGENT, MODEL 10220?

The FDA product code for EASYRA MG REAGENT, MODEL 10220 is JGJ.

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Related Devices (Code: JGJ)

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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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