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FDA 510(k)

BOARD, DISPOSABLE CONTROL COUNT

K-Number: K781791 · 1978-11-08

ApplicantDexide, Inc.
Decision Date1978-11-08
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOARD, DISPOSABLE CONTROL COUNT is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1978-11-08 under 510(k) number K781791. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOARD, DISPOSABLE CONTROL COUNT?

BOARD, DISPOSABLE CONTROL COUNT is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Dexide, Inc.. The 510(k) number is K781791.

When did BOARD, DISPOSABLE CONTROL COUNT receive FDA 510(k) clearance?

BOARD, DISPOSABLE CONTROL COUNT received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781791.

Who is the listed applicant for BOARD, DISPOSABLE CONTROL COUNT?

The FDA 510(k) record lists Dexide, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOARD, DISPOSABLE CONTROL COUNT?

The FDA product code for BOARD, DISPOSABLE CONTROL COUNT is MMK.

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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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