Megapulse III Shortwave Diathermy
K-Number: K153456 · 2016-06-14
ApplicantAccelerated Care Plus
Decision Date2016-06-14
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Megapulse III Shortwave Diathermy is a medical device manufactured by Accelerated Care Plus. It received FDA 510(k) clearance on 2016-06-14 under approval number K153456. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Megapulse III Shortwave Diathermy?
Megapulse III Shortwave Diathermy is a medical device that received FDA 510(k) clearance on 2016-06-14. It is manufactured by Accelerated Care Plus. The 510(k) number is K153456.
When was Megapulse III Shortwave Diathermy approved by the FDA?
Megapulse III Shortwave Diathermy received FDA 510(k) clearance on 2016-06-14, under approval number K153456.
What company makes Megapulse III Shortwave Diathermy?
Megapulse III Shortwave Diathermy is manufactured by Accelerated Care Plus.
What is the FDA product code for Megapulse III Shortwave Diathermy?
The FDA product code for Megapulse III Shortwave Diathermy is IMJ.
Related Clinical Trials
Related Devices (Code: IMJ)
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.