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FDA 510(k)

COMPACT PIEZO P2K, POWERCARE

K-Number: K102218 · 2011-01-24

ApplicantMectron S.P.A.
Decision Date2011-01-24
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPACT PIEZO P2K, POWERCARE is the device name listed in this FDA 510(k) record. The listed applicant is Mectron S.P.A.. It received FDA 510(k) clearance on 2011-01-24 under 510(k) number K102218. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPACT PIEZO P2K, POWERCARE?

COMPACT PIEZO P2K, POWERCARE is a medical device that received FDA 510(k) clearance on 2011-01-24. The listed applicant is Mectron S.P.A.. The 510(k) number is K102218.

When did COMPACT PIEZO P2K, POWERCARE receive FDA 510(k) clearance?

COMPACT PIEZO P2K, POWERCARE received FDA 510(k) clearance on 2011-01-24, under 510(k) number K102218.

Who is the listed applicant for COMPACT PIEZO P2K, POWERCARE?

The FDA 510(k) record lists Mectron S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPACT PIEZO P2K, POWERCARE?

The FDA product code for COMPACT PIEZO P2K, POWERCARE is ELC.

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Related Devices (Code: ELC)

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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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