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FDA 510(k)

MIC-2000 INOCULATOR TEMPLATE

K-Number: K790974 · 1979-06-20

ApplicantDynatech Laboratories, Inc.
Decision Date1979-06-20
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIC-2000 INOCULATOR TEMPLATE 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 1979-06-20 under 510(k) number K790974. 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 MIC-2000 INOCULATOR TEMPLATE?

MIC-2000 INOCULATOR TEMPLATE is a medical device that received FDA 510(k) clearance on 1979-06-20. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K790974.

When did MIC-2000 INOCULATOR TEMPLATE receive FDA 510(k) clearance?

MIC-2000 INOCULATOR TEMPLATE received FDA 510(k) clearance on 1979-06-20, under 510(k) number K790974.

Who is the listed applicant for MIC-2000 INOCULATOR TEMPLATE?

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 MIC-2000 INOCULATOR TEMPLATE?

The FDA product code for MIC-2000 INOCULATOR TEMPLATE is JTC.

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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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