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FDA 510(k)

D-Actor 200 Vibration Massage System

K-Number: K173692 · 2018-04-13

ApplicantStorz Medical AG
Decision Date2018-04-13
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

D-Actor 200 Vibration Massage System is a medical device manufactured by Storz Medical AG. It received FDA 510(k) clearance on 2018-04-13 under approval number K173692. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D-Actor 200 Vibration Massage System?

D-Actor 200 Vibration Massage System is a medical device that received FDA 510(k) clearance on 2018-04-13. It is manufactured by Storz Medical AG. The 510(k) number is K173692.

When was D-Actor 200 Vibration Massage System approved by the FDA?

D-Actor 200 Vibration Massage System received FDA 510(k) clearance on 2018-04-13, under approval number K173692.

What company makes D-Actor 200 Vibration Massage System?

D-Actor 200 Vibration Massage System is manufactured by Storz Medical AG.

What is the FDA product code for D-Actor 200 Vibration Massage System?

The FDA product code for D-Actor 200 Vibration Massage System is ISA.

Related Clinical Trials

NCT07556198 Effects of Whole-Body Vibration With Foot Core Exercises: A Randomized Controlled Trial COMPLETED NCT07529678 Differences in Autonomic Recovery Between Physically Active and Inactive Women Following an Automated Massage Chair Intervention COMPLETED NCT06845176 Combining Motor Imagery and Tendon Vibration on the Effectiveness of Motor Imagery RECRUITING

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K203710Storz Medical MAGNETOLITH Muscle Stimulator K202112Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece PMA P080028Generator, shock-wave, for pain relief

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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.

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