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FDA 510(k)

MUSCLE DYSFUNCTION MONITOR

K-Number: K820568 · 1982-04-09

ApplicantA Company, Inc.
Decision Date1982-04-09
Product CodeDZM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MUSCLE DYSFUNCTION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is A Company, Inc.. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820568. The device is classified under product code DZM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSCLE DYSFUNCTION MONITOR?

MUSCLE DYSFUNCTION MONITOR is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is A Company, Inc.. The 510(k) number is K820568.

When did MUSCLE DYSFUNCTION MONITOR receive FDA 510(k) clearance?

MUSCLE DYSFUNCTION MONITOR received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820568.

Who is the listed applicant for MUSCLE DYSFUNCTION MONITOR?

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

What is the FDA product code for MUSCLE DYSFUNCTION MONITOR?

The FDA product code for MUSCLE DYSFUNCTION MONITOR is DZM.

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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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