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FDA 510(k)

THE MYOLOC SYSTEM

K-Number: K900678 · 1990-08-13

ApplicantWinder Research, Inc.
Decision Date1990-08-13
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE MYOLOC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Winder Research, Inc.. It received FDA 510(k) clearance on 1990-08-13 under 510(k) number K900678. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MYOLOC SYSTEM?

THE MYOLOC SYSTEM is a medical device that received FDA 510(k) clearance on 1990-08-13. The listed applicant is Winder Research, Inc.. The 510(k) number is K900678.

When did THE MYOLOC SYSTEM receive FDA 510(k) clearance?

THE MYOLOC SYSTEM received FDA 510(k) clearance on 1990-08-13, under 510(k) number K900678.

Who is the listed applicant for THE MYOLOC SYSTEM?

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

What is the FDA product code for THE MYOLOC SYSTEM?

The FDA product code for THE MYOLOC SYSTEM is EJF.

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Related Devices (Code: EJF)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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