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FDA 510(k)

MUSCLE PAIN DEVICE (MPD)

K-Number: K073361 · 2008-03-18

ApplicantStevens Proof of Concept, Inc.
Decision Date2008-03-18
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCLE PAIN DEVICE (MPD) is the device name listed in this FDA 510(k) record. The listed applicant is Stevens Proof of Concept, Inc.. It received FDA 510(k) clearance on 2008-03-18 under 510(k) number K073361. 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 MUSCLE PAIN DEVICE (MPD)?

MUSCLE PAIN DEVICE (MPD) is a medical device that received FDA 510(k) clearance on 2008-03-18. The listed applicant is Stevens Proof of Concept, Inc.. The 510(k) number is K073361.

When did MUSCLE PAIN DEVICE (MPD) receive FDA 510(k) clearance?

MUSCLE PAIN DEVICE (MPD) received FDA 510(k) clearance on 2008-03-18, under 510(k) number K073361.

Who is the listed applicant for MUSCLE PAIN DEVICE (MPD)?

The FDA 510(k) record lists Stevens Proof of Concept, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUSCLE PAIN DEVICE (MPD)?

The FDA product code for MUSCLE PAIN DEVICE (MPD) is IPF.

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Related Devices (Code: 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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