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FDA 510(k)

MR 600 MICROPLATE READER

K-Number: K821439 · 1982-06-01

Decision Date1982-06-01
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MR 600 MICROPLATE READER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1982-06-01 under 510(k) number K821439. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR 600 MICROPLATE READER?

MR 600 MICROPLATE READER is a medical device that received FDA 510(k) clearance on 1982-06-01. The listed applicant is Dynatech Corp.. The 510(k) number is K821439.

When did MR 600 MICROPLATE READER receive FDA 510(k) clearance?

MR 600 MICROPLATE READER received FDA 510(k) clearance on 1982-06-01, under 510(k) number K821439.

Who is the listed applicant for MR 600 MICROPLATE READER?

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

What is the FDA product code for MR 600 MICROPLATE READER?

The FDA product code for MR 600 MICROPLATE READER is JJQ.

Related Clinical Trials

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.

Other records listing Dynatech 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.

View all 27 devices →

Related Devices (Code: JJQ)

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.

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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