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FDA 510(k)

Grivamax Hair Growth System

K-Number: K171895 · 2017-08-22

Decision Date2017-08-22
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Grivamax Hair Growth System is the device name listed in this FDA 510(k) record. The listed applicant is Leana Orders, Inc.. It received FDA 510(k) clearance on 2017-08-22 under 510(k) number K171895. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Grivamax Hair Growth System?

Grivamax Hair Growth System is a medical device that received FDA 510(k) clearance on 2017-08-22. The listed applicant is Leana Orders, Inc.. The 510(k) number is K171895.

When did Grivamax Hair Growth System receive FDA 510(k) clearance?

Grivamax Hair Growth System received FDA 510(k) clearance on 2017-08-22, under 510(k) number K171895.

Who is the listed applicant for Grivamax Hair Growth System?

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

What is the FDA product code for Grivamax Hair Growth System?

The FDA product code for Grivamax Hair Growth System is OAP.

Other records listing Leana Orders, 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.

Related Devices (Code: OAP)

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.

Official Source

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