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FDA 510(k)

DYNATECH MR 300 MANUAL MICROELISA

K-Number: K874244 · 1987-11-03

ApplicantDynatech Laboratories, Inc.
Decision Date1987-11-03
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DYNATECH MR 300 MANUAL MICROELISA is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1987-11-03 under 510(k) number K874244. 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 DYNATECH MR 300 MANUAL MICROELISA?

DYNATECH MR 300 MANUAL MICROELISA is a medical device that received FDA 510(k) clearance on 1987-11-03. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K874244.

When did DYNATECH MR 300 MANUAL MICROELISA receive FDA 510(k) clearance?

DYNATECH MR 300 MANUAL MICROELISA received FDA 510(k) clearance on 1987-11-03, under 510(k) number K874244.

Who is the listed applicant for DYNATECH MR 300 MANUAL MICROELISA?

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

What is the FDA product code for DYNATECH MR 300 MANUAL MICROELISA?

The FDA product code for DYNATECH MR 300 MANUAL MICROELISA is JJQ.

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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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