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FDA 510(k)

HISTO-DISPENSER

K-Number: K790957 · 1979-06-15

ApplicantDynatech Laboratories, Inc.
Decision Date1979-06-15
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HISTO-DISPENSER 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 1979-06-15 under 510(k) number K790957. 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 HISTO-DISPENSER?

HISTO-DISPENSER is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K790957.

When did HISTO-DISPENSER receive FDA 510(k) clearance?

HISTO-DISPENSER received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790957.

Who is the listed applicant for HISTO-DISPENSER?

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 HISTO-DISPENSER?

The FDA product code for HISTO-DISPENSER is JTC.

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Related Devices (Code: 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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