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FDA 510(k)

BODYFLOW P2CH

K-Number: K100862 · 2011-04-21

ApplicantPhysiomed Elektromedizin AG
Decision Date2011-04-21
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BODYFLOW P2CH is the device name listed in this FDA 510(k) record. The listed applicant is Physiomed Elektromedizin AG. It received FDA 510(k) clearance on 2011-04-21 under 510(k) number K100862. 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 BODYFLOW P2CH?

BODYFLOW P2CH is a medical device that received FDA 510(k) clearance on 2011-04-21. The listed applicant is Physiomed Elektromedizin AG. The 510(k) number is K100862.

When did BODYFLOW P2CH receive FDA 510(k) clearance?

BODYFLOW P2CH received FDA 510(k) clearance on 2011-04-21, under 510(k) number K100862.

Who is the listed applicant for BODYFLOW P2CH?

The FDA 510(k) record lists Physiomed Elektromedizin AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BODYFLOW P2CH?

The FDA product code for BODYFLOW P2CH is IPF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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