FDA 510(k)

PERCUSSIVETECH HF, MODEL 2001

K-Number: K981726 · 1998-09-17

ApplicantVortran Medical Technology 1, Inc.

Decision Date1998-09-17

Product CodeNHJ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PERCUSSIVETECH HF, MODEL 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 1998-09-17 under 510(k) number K981726. The device is classified under product code NHJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUSSIVETECH HF, MODEL 2001?

PERCUSSIVETECH HF, MODEL 2001 is a medical device that received FDA 510(k) clearance on 1998-09-17. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K981726.

When did PERCUSSIVETECH HF, MODEL 2001 receive FDA 510(k) clearance?

PERCUSSIVETECH HF, MODEL 2001 received FDA 510(k) clearance on 1998-09-17, under 510(k) number K981726.

Who is the listed applicant for PERCUSSIVETECH HF, MODEL 2001?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUSSIVETECH HF, MODEL 2001?

The FDA product code for PERCUSSIVETECH HF, MODEL 2001 is NHJ.

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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.