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FDA 510(k)

LYMPHA PRESS 201MAX, MODEL 201MAX

K-Number: K100677 · 2010-05-20

ApplicantMego Afek AC , Ltd.
Decision Date2010-05-20
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LYMPHA PRESS 201MAX, MODEL 201MAX is the device name listed in this FDA 510(k) record. The listed applicant is Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2010-05-20 under 510(k) number K100677. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYMPHA PRESS 201MAX, MODEL 201MAX?

LYMPHA PRESS 201MAX, MODEL 201MAX is a medical device that received FDA 510(k) clearance on 2010-05-20. The listed applicant is Mego Afek AC , Ltd.. The 510(k) number is K100677.

When did LYMPHA PRESS 201MAX, MODEL 201MAX receive FDA 510(k) clearance?

LYMPHA PRESS 201MAX, MODEL 201MAX received FDA 510(k) clearance on 2010-05-20, under 510(k) number K100677.

Who is the listed applicant for LYMPHA PRESS 201MAX, MODEL 201MAX?

The FDA 510(k) record lists Mego Afek AC , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYMPHA PRESS 201MAX, MODEL 201MAX?

The FDA product code for LYMPHA PRESS 201MAX, MODEL 201MAX is JOW.

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Related Devices (Code: JOW)

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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