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FDA 510(k)

Pulse Aloe-ahh

K-Number: K152671 · 2016-07-11

Decision Date2016-07-11
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Pulse Aloe-ahh is the device name listed in this FDA 510(k) record. The listed applicant is Toaster Labs, Inc.. It received FDA 510(k) clearance on 2016-07-11 under 510(k) 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. 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

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