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FDA 510(k)

METRON-CP/MD

K-Number: K103554 · 2011-12-20

ApplicantEponatech, LLC
Decision Date2011-12-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

METRON-CP/MD is the device name listed in this FDA 510(k) record. The listed applicant is Eponatech, LLC. It received FDA 510(k) clearance on 2011-12-20 under 510(k) number K103554. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRON-CP/MD?

METRON-CP/MD is a medical device that received FDA 510(k) clearance on 2011-12-20. The listed applicant is Eponatech, LLC. The 510(k) number is K103554.

When did METRON-CP/MD receive FDA 510(k) clearance?

METRON-CP/MD received FDA 510(k) clearance on 2011-12-20, under 510(k) number K103554.

Who is the listed applicant for METRON-CP/MD?

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

What is the FDA product code for METRON-CP/MD?

The FDA product code for METRON-CP/MD is LLZ.

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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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