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FDA 510(k)

INOCULATOR, MIC-2000 DISPOSABLE

K-Number: K790076 · 1979-02-01

Decision Date1979-02-01
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

INOCULATOR, MIC-2000 DISPOSABLE 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 1979-02-01 under 510(k) number K790076. 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 INOCULATOR, MIC-2000 DISPOSABLE?

INOCULATOR, MIC-2000 DISPOSABLE is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K790076.

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

INOCULATOR, MIC-2000 DISPOSABLE received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790076.

Who is the listed applicant for INOCULATOR, MIC-2000 DISPOSABLE?

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 INOCULATOR, MIC-2000 DISPOSABLE?

The FDA product code for INOCULATOR, MIC-2000 DISPOSABLE 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 Laboratories, Inc. 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 44 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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