Pulse Aloe-ahh
K-Number: K152671 · 2016-07-11
Device Summary
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. The listed applicant is Toaster Labs, Inc.. The 510(k) number is K152671.
When did Pulse Aloe-ahh receive FDA 510(k) clearance?
Pulse Aloe-ahh received FDA 510(k) clearance on 2016-07-11, under 510(k) number K152671.
Who is the listed applicant for Pulse Aloe-ahh?
The FDA 510(k) record lists Toaster Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pulse Aloe-ahh?
The FDA product code for Pulse Aloe-ahh is NUC.
Other records listing Toaster Labs, 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: NUC)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.