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FDA 510(k)

MANUAL MICRO ELISA READER #2-530

K-Number: K791302 · 1979-08-16

ApplicantDynatech Laboratories, Inc.
Decision Date1979-08-16
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MANUAL MICRO ELISA READER #2-530 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 1979-08-16 under 510(k) number K791302. 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 MANUAL MICRO ELISA READER #2-530?

MANUAL MICRO ELISA READER #2-530 is a medical device that received FDA 510(k) clearance on 1979-08-16. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K791302.

When did MANUAL MICRO ELISA READER #2-530 receive FDA 510(k) clearance?

MANUAL MICRO ELISA READER #2-530 received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791302.

Who is the listed applicant for MANUAL MICRO ELISA READER #2-530?

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 MANUAL MICRO ELISA READER #2-530?

The FDA product code for MANUAL MICRO ELISA READER #2-530 is JJQ.

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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.

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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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