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FDA 510(k)

DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER

K-Number: K872199 · 1987-08-21

ApplicantDyno-Max Co.
Decision Date1987-08-21
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Dyno-Max Co.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872199. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER?

DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Dyno-Max Co.. The 510(k) number is K872199.

When did DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER receive FDA 510(k) clearance?

DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872199.

Who is the listed applicant for DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER?

The FDA 510(k) record lists Dyno-Max Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER?

The FDA product code for DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER is IKK.

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Related Devices (Code: IKK)

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.

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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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