Dermiview Hypoallergenic Clear Tape

FDA 510(k) K944587 · Johnson & Johnson Medical, Inc.

Substantially Equivalent

510(k) numberK944587

Submission

Device name
Dermiview Hypoallergenic Clear Tape
Applicant
Johnson & Johnson Medical, Inc.
Arlington, TX, US
Received
September 19, 1994
Decision date
October 30, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KGX – Tape And Bandage, Adhesive
Device class
Class I (low risk)
Regulation
21 CFR 880.5240
Specialty
General Hospital

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K954007ParallelKGX · Traditional Johnson & Johnson Consumer Products, Inc.11/22/1995SE
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K940536Band-Aid(Tm) Brand Adhesive BandageKGX · Traditional Johnson & Johnson Consumer Products, Inc.10/03/1994SE
K940798Shippert Pressure BandageKGX · Traditional Denver Splint Co.09/28/1994SE

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Questions and answers

When was Dermiview Hypoallergenic Clear Tape cleared by the FDA?

Dermiview Hypoallergenic Clear Tape (K944587) received a 510(k) decision of Substantially Equivalent on October 30, 1995, 406 days after the submission was received.

What is the product code of K944587?

The FDA product code is KGX – Tape And Bandage, Adhesive, a Class I (low risk) device regulated under 21 CFR 880.5240.