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FDA 510(k)

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S

K-Number: K050046 · 2005-04-13

ApplicantCompex Technologies, Inc.
Decision Date2005-04-13
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S is the device name listed in this FDA 510(k) record. The listed applicant is Compex Technologies, Inc.. It received FDA 510(k) clearance on 2005-04-13 under 510(k) number K050046. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S?

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S is a medical device that received FDA 510(k) clearance on 2005-04-13. The listed applicant is Compex Technologies, Inc.. The 510(k) number is K050046.

When did REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S receive FDA 510(k) clearance?

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S received FDA 510(k) clearance on 2005-04-13, under 510(k) number K050046.

Who is the listed applicant for REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S?

The FDA 510(k) record lists Compex Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S?

The FDA product code for REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S is IPF.

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Other records listing Compex Technologies, Inc. as applicant

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Official Source

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