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FDA 510(k)

SuperGrow 272, Ultimate 272

K-Number: K181308 · 2018-08-15

ApplicantSuper Grow Lasers
Decision Date2018-08-15
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SuperGrow 272, Ultimate 272 is the device name listed in this FDA 510(k) record. The listed applicant is Super Grow Lasers. It received FDA 510(k) clearance on 2018-08-15 under 510(k) number K181308. 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 SuperGrow 272, Ultimate 272?

SuperGrow 272, Ultimate 272 is a medical device that received FDA 510(k) clearance on 2018-08-15. The listed applicant is Super Grow Lasers. The 510(k) number is K181308.

When did SuperGrow 272, Ultimate 272 receive FDA 510(k) clearance?

SuperGrow 272, Ultimate 272 received FDA 510(k) clearance on 2018-08-15, under 510(k) number K181308.

Who is the listed applicant for SuperGrow 272, Ultimate 272?

The FDA 510(k) record lists Super Grow Lasers as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SuperGrow 272, Ultimate 272?

The FDA product code for SuperGrow 272, Ultimate 272 is OAP.

Other records listing Super Grow Lasers 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.

K172982SuperGrow 272, Ultimate 272

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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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