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FDA 510(k)

OMNISTIM III INTERFERENTIAL THERAPY

K-Number: K841278 · 1984-04-24

ApplicantPhysio Technology, Inc.
Decision Date1984-04-24
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OMNISTIM III INTERFERENTIAL THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Physio Technology, Inc.. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K841278. 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 OMNISTIM III INTERFERENTIAL THERAPY?

OMNISTIM III INTERFERENTIAL THERAPY is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Physio Technology, Inc.. The 510(k) number is K841278.

When did OMNISTIM III INTERFERENTIAL THERAPY receive FDA 510(k) clearance?

OMNISTIM III INTERFERENTIAL THERAPY received FDA 510(k) clearance on 1984-04-24, under 510(k) number K841278.

Who is the listed applicant for OMNISTIM III INTERFERENTIAL THERAPY?

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

What is the FDA product code for OMNISTIM III INTERFERENTIAL THERAPY?

The FDA product code for OMNISTIM III INTERFERENTIAL THERAPY is IPF.

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Related Devices (Code: IPF)

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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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