Pulse Aloe-ahh
K-Number: K152671 · 2016-07-11
ApplicantToaster Labs, Inc.
Decision Date2016-07-11
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Pulse Aloe-ahh is a medical device manufactured by Toaster Labs, Inc.. It received FDA 510(k) clearance on 2016-07-11 under approval number K152671. 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 Aloe-ahh?
Pulse Aloe-ahh 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 K152671.
When was Pulse Aloe-ahh approved by the FDA?
Pulse Aloe-ahh received FDA 510(k) clearance on 2016-07-11, under approval number K152671.
What company makes Pulse Aloe-ahh?
Pulse Aloe-ahh is manufactured by Toaster Labs, Inc..
What is the FDA product code for Pulse Aloe-ahh?
The FDA product code for Pulse Aloe-ahh is NUC.
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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.