AliTight

FDA 510(k) K231146 · Alic Iotech, LLC

Substantially Equivalent

510(k) numberK231146

Submission

Device name
AliTight
Applicant
Alic Iotech, LLC
Pleasanton, CA, US
Received
April 21, 2023
Decision date
September 8, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEI – Electrosurgical, Cutting & Coagulation & Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4400
Specialty
General, Plastic Surgery

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was AliTight cleared by the FDA?

AliTight (K231146) received a 510(k) decision of Substantially Equivalent on September 8, 2023, 140 days after the submission was received.

What is the product code of K231146?

The FDA product code is GEI – Electrosurgical, Cutting & Coagulation & Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4400.