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FDA 510(k)

MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS

K-Number: K013905 · 2002-04-22

ApplicantPro-Tech Services, Inc.
Decision Date2002-04-22
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tech Services, Inc.. It received FDA 510(k) clearance on 2002-04-22 under 510(k) number K013905. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS?

MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS is a medical device that received FDA 510(k) clearance on 2002-04-22. The listed applicant is Pro-Tech Services, Inc.. The 510(k) number is K013905.

When did MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS receive FDA 510(k) clearance?

MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS received FDA 510(k) clearance on 2002-04-22, under 510(k) number K013905.

Who is the listed applicant for MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS?

The FDA 510(k) record lists Pro-Tech Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS?

The FDA product code for MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS is MNR.

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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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