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FDA 510(k)

PROTRON TECHNOLOGIES, LLC STETHOTRON

K-Number: K082771 · 2009-02-27

ApplicantProtron Technologies, LLC
Decision Date2009-02-27
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROTRON TECHNOLOGIES, LLC STETHOTRON is the device name listed in this FDA 510(k) record. The listed applicant is Protron Technologies, LLC. It received FDA 510(k) clearance on 2009-02-27 under 510(k) number K082771. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTRON TECHNOLOGIES, LLC STETHOTRON?

PROTRON TECHNOLOGIES, LLC STETHOTRON is a medical device that received FDA 510(k) clearance on 2009-02-27. The listed applicant is Protron Technologies, LLC. The 510(k) number is K082771.

When did PROTRON TECHNOLOGIES, LLC STETHOTRON receive FDA 510(k) clearance?

PROTRON TECHNOLOGIES, LLC STETHOTRON received FDA 510(k) clearance on 2009-02-27, under 510(k) number K082771.

Who is the listed applicant for PROTRON TECHNOLOGIES, LLC STETHOTRON?

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

What is the FDA product code for PROTRON TECHNOLOGIES, LLC STETHOTRON?

The FDA product code for PROTRON TECHNOLOGIES, LLC STETHOTRON is DQD.

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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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