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FDA 510(k)

PIPER IPPB MODEL 2055

K-Number: K982016 · 1998-11-03

ApplicantVortran Medical Technology 1, Inc.
Decision Date1998-11-03
Product CodeNHJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PIPER IPPB MODEL 2055 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 1998-11-03 under 510(k) number K982016. 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 PIPER IPPB MODEL 2055?

PIPER IPPB MODEL 2055 is a medical device that received FDA 510(k) clearance on 1998-11-03. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K982016.

When did PIPER IPPB MODEL 2055 receive FDA 510(k) clearance?

PIPER IPPB MODEL 2055 received FDA 510(k) clearance on 1998-11-03, under 510(k) number K982016.

Who is the listed applicant for PIPER IPPB MODEL 2055?

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 PIPER IPPB MODEL 2055?

The FDA product code for PIPER IPPB MODEL 2055 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.

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