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FDA 510(k)

MIC-2000 PLUS, 96 CHANNEL DISPENSER

K-Number: K820821 · 1982-04-14

Decision Date1982-04-14
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIC-2000 PLUS, 96 CHANNEL DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1982-04-14 under 510(k) number K820821. 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 PLUS, 96 CHANNEL DISPENSER?

MIC-2000 PLUS, 96 CHANNEL DISPENSER is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is Dynatech Corp.. The 510(k) number is K820821.

When did MIC-2000 PLUS, 96 CHANNEL DISPENSER receive FDA 510(k) clearance?

MIC-2000 PLUS, 96 CHANNEL DISPENSER received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820821.

Who is the listed applicant for MIC-2000 PLUS, 96 CHANNEL DISPENSER?

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 MIC-2000 PLUS, 96 CHANNEL DISPENSER?

The FDA product code for MIC-2000 PLUS, 96 CHANNEL DISPENSER is JTC.

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: 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.

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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