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FDA 510(k)

PAINSHIELD MD

K-Number: K081075 · 2008-08-22

ApplicantNano Vibronix , Ltd.
Decision Date2008-08-22
Product CodePFW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PAINSHIELD MD is the device name listed in this FDA 510(k) record. The listed applicant is Nano Vibronix , Ltd.. It received FDA 510(k) clearance on 2008-08-22 under 510(k) number K081075. The device is classified under product code PFW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAINSHIELD MD?

PAINSHIELD MD is a medical device that received FDA 510(k) clearance on 2008-08-22. The listed applicant is Nano Vibronix , Ltd.. The 510(k) number is K081075.

When did PAINSHIELD MD receive FDA 510(k) clearance?

PAINSHIELD MD received FDA 510(k) clearance on 2008-08-22, under 510(k) number K081075.

Who is the listed applicant for PAINSHIELD MD?

The FDA 510(k) record lists Nano Vibronix , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAINSHIELD MD?

The FDA product code for PAINSHIELD MD is PFW.

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Related Devices (Code: PFW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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