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FDA 510(k)

MAGO AUTOMATED EIA PROCESSOR

K-Number: K973177 · 1997-10-09

ApplicantDiamedix Corp.
Decision Date1997-10-09
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGO AUTOMATED EIA PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Diamedix Corp.. It received FDA 510(k) clearance on 1997-10-09 under 510(k) number K973177. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGO AUTOMATED EIA PROCESSOR?

MAGO AUTOMATED EIA PROCESSOR is a medical device that received FDA 510(k) clearance on 1997-10-09. The listed applicant is Diamedix Corp.. The 510(k) number is K973177.

When did MAGO AUTOMATED EIA PROCESSOR receive FDA 510(k) clearance?

MAGO AUTOMATED EIA PROCESSOR received FDA 510(k) clearance on 1997-10-09, under 510(k) number K973177.

Who is the listed applicant for MAGO AUTOMATED EIA PROCESSOR?

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

What is the FDA product code for MAGO AUTOMATED EIA PROCESSOR?

The FDA product code for MAGO AUTOMATED EIA PROCESSOR is JJF.

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Other records listing Diamedix Corp. 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.

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Related Devices (Code: JJF)

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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