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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 a medical device manufactured by Super Grow Lasers. It received FDA 510(k) clearance on 2018-08-15 under approval 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. It is manufactured by Super Grow Lasers. The 510(k) number is K181308.

When was SuperGrow 272, Ultimate 272 approved by the FDA?

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

What company makes SuperGrow 272, Ultimate 272?

SuperGrow 272, Ultimate 272 is manufactured by Super Grow Lasers.

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

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

Other Devices by Super Grow Lasers

K172982SuperGrow 272, Ultimate 272

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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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