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FDA 510(k)

DEFIBRILLATOR CABLE TESTER, MODEL DT2200

K-Number: K061606 · 2006-06-21

ApplicantMedical Devices/Padpro, Inc.
Decision Date2006-06-21
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEFIBRILLATOR CABLE TESTER, MODEL DT2200 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices/Padpro, Inc.. It received FDA 510(k) clearance on 2006-06-21 under 510(k) number K061606. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFIBRILLATOR CABLE TESTER, MODEL DT2200?

DEFIBRILLATOR CABLE TESTER, MODEL DT2200 is a medical device that received FDA 510(k) clearance on 2006-06-21. The listed applicant is Medical Devices/Padpro, Inc.. The 510(k) number is K061606.

When did DEFIBRILLATOR CABLE TESTER, MODEL DT2200 receive FDA 510(k) clearance?

DEFIBRILLATOR CABLE TESTER, MODEL DT2200 received FDA 510(k) clearance on 2006-06-21, under 510(k) number K061606.

Who is the listed applicant for DEFIBRILLATOR CABLE TESTER, MODEL DT2200?

The FDA 510(k) record lists Medical Devices/Padpro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFIBRILLATOR CABLE TESTER, MODEL DT2200?

The FDA product code for DEFIBRILLATOR CABLE TESTER, MODEL DT2200 is DRG.

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Related Devices (Code: DRG)

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

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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