Apyx
K-Number: K230730 · 2023-07-25
ApplicantEscala Medical
Decision Date2023-07-25
Product CodePBQ
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Apyx is a medical device manufactured by Escala Medical. It received FDA 510(k) clearance on 2023-07-25 under approval number K230730. The device is classified under product code PBQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Apyx?
Apyx is a medical device that received FDA 510(k) clearance on 2023-07-25. It is manufactured by Escala Medical. The 510(k) number is K230730.
When was Apyx approved by the FDA?
Apyx received FDA 510(k) clearance on 2023-07-25, under approval number K230730.
What company makes Apyx?
Apyx is manufactured by Escala Medical.
What is the FDA product code for Apyx?
The FDA product code for Apyx is PBQ.
Other Devices by Escala Medical
Related Devices (Code: PBQ)
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.