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FDA 510(k)

HAUSTED POWERTRAN SERIES STRETCHER

K-Number: K041924 · 2004-09-09

ApplicantSTERIS Corporation
Decision Date2004-09-09
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAUSTED POWERTRAN SERIES STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2004-09-09 under 510(k) number K041924. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAUSTED POWERTRAN SERIES STRETCHER?

HAUSTED POWERTRAN SERIES STRETCHER is a medical device that received FDA 510(k) clearance on 2004-09-09. The listed applicant is STERIS Corporation. The 510(k) number is K041924.

When did HAUSTED POWERTRAN SERIES STRETCHER receive FDA 510(k) clearance?

HAUSTED POWERTRAN SERIES STRETCHER received FDA 510(k) clearance on 2004-09-09, under 510(k) number K041924.

Who is the listed applicant for HAUSTED POWERTRAN SERIES STRETCHER?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAUSTED POWERTRAN SERIES STRETCHER?

The FDA product code for HAUSTED POWERTRAN SERIES STRETCHER is INK.

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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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