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FDA 510(k)

VERIMED MYOEXORCISER III (MYO III)

K-Number: K892649 · 1989-12-13

ApplicantVerimed Holdings, Inc.
Decision Date1989-12-13
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERIMED MYOEXORCISER III (MYO III) is the device name listed in this FDA 510(k) record. The listed applicant is Verimed Holdings, Inc.. It received FDA 510(k) clearance on 1989-12-13 under 510(k) number K892649. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIMED MYOEXORCISER III (MYO III)?

VERIMED MYOEXORCISER III (MYO III) is a medical device that received FDA 510(k) clearance on 1989-12-13. The listed applicant is Verimed Holdings, Inc.. The 510(k) number is K892649.

When did VERIMED MYOEXORCISER III (MYO III) receive FDA 510(k) clearance?

VERIMED MYOEXORCISER III (MYO III) received FDA 510(k) clearance on 1989-12-13, under 510(k) number K892649.

Who is the listed applicant for VERIMED MYOEXORCISER III (MYO III)?

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

What is the FDA product code for VERIMED MYOEXORCISER III (MYO III)?

The FDA product code for VERIMED MYOEXORCISER III (MYO III) is HCC.

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Other records listing Verimed Holdings, Inc. as applicant

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.

K981277PERIFORMK954127BIOFEEDBACK DEVICEK951969MYOEXORCISER II FUALK930670PHYACTION 787K922550ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)K913912VERIMED PERINEOMETER

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Related Devices (Code: HCC)

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.

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, LLC

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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