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FDA 510(k)

DYNATECH MR 250 MANUAL MICROELISA READER

K-Number: K874598 · 1987-11-20

ApplicantDynatech Laboratories, Inc.
Decision Date1987-11-20
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DYNATECH MR 250 MANUAL MICROELISA READER 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 1987-11-20 under 510(k) number K874598. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATECH MR 250 MANUAL MICROELISA READER?

DYNATECH MR 250 MANUAL MICROELISA READER is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K874598.

When did DYNATECH MR 250 MANUAL MICROELISA READER receive FDA 510(k) clearance?

DYNATECH MR 250 MANUAL MICROELISA READER received FDA 510(k) clearance on 1987-11-20, under 510(k) number K874598.

Who is the listed applicant for DYNATECH MR 250 MANUAL MICROELISA READER?

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 250 MANUAL MICROELISA READER?

The FDA product code for DYNATECH MR 250 MANUAL MICROELISA READER is JTC.

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Other records listing Dynatech Laboratories, Inc. as applicant

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Related Devices (Code: JTC)

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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