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FDA 510(k)

DAYTRIPPER DIALYSATE WARMER

K-Number: K020542 · 2002-09-27

ApplicantStickman Industries, Inc.
Decision Date2002-09-27
Product CodeMLW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAYTRIPPER DIALYSATE WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Stickman Industries, Inc.. It received FDA 510(k) clearance on 2002-09-27 under 510(k) number K020542. The device is classified under product code MLW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAYTRIPPER DIALYSATE WARMER?

DAYTRIPPER DIALYSATE WARMER is a medical device that received FDA 510(k) clearance on 2002-09-27. The listed applicant is Stickman Industries, Inc.. The 510(k) number is K020542.

When did DAYTRIPPER DIALYSATE WARMER receive FDA 510(k) clearance?

DAYTRIPPER DIALYSATE WARMER received FDA 510(k) clearance on 2002-09-27, under 510(k) number K020542.

Who is the listed applicant for DAYTRIPPER DIALYSATE WARMER?

The FDA 510(k) record lists Stickman Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAYTRIPPER DIALYSATE WARMER?

The FDA product code for DAYTRIPPER DIALYSATE WARMER is MLW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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