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FDA 510(k)

Pulse H20h!

K-Number: K152628 · 2016-07-11

ApplicantToaster Labs, Inc.
Decision Date2016-07-11
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Pulse H20h! is a medical device manufactured by Toaster Labs, Inc.. It received FDA 510(k) clearance on 2016-07-11 under approval number K152628. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pulse H20h!?

Pulse H20h! is a medical device that received FDA 510(k) clearance on 2016-07-11. It is manufactured by Toaster Labs, Inc.. The 510(k) number is K152628.

When was Pulse H20h! approved by the FDA?

Pulse H20h! received FDA 510(k) clearance on 2016-07-11, under approval number K152628.

What company makes Pulse H20h!?

Pulse H20h! is manufactured by Toaster Labs, Inc..

What is the FDA product code for Pulse H20h!?

The FDA product code for Pulse H20h! is NUC.

Other Devices by Toaster Labs, Inc.

K152671Pulse Aloe-ahh

Related Devices (Code: NUC)

K161585Mano and Mano Personal LubricantMano and Mano Proprietary Limited K161544Trojan Chain Reaction Personal LubricantChurch & Dwight Co., Inc. K161385Just Like Me Personal LubricantWtfn-Dba Classic Erotica/Holiday Products K152671Pulse Aloe-ahhToaster Labs, Inc. K153372Repagyn vaginal suppositoriesFarma-Derma S.R.L. K160763ally Liquid Personal LubricantPrivate Label Production, 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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