Scanlan Colormark Skin Marker

FDA 510(k) K841085 · Scanlan Intl., Inc.

Substantially Equivalent

510(k) numberK841085

Submission

Device name
Scanlan Colormark Skin Marker
Applicant
Scanlan Intl., Inc.
Mchenry, IL, US
Received
March 13, 1984
Decision date
June 11, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FZZ – Marker, Skin
Device class
Class I (low risk)
Regulation
21 CFR 878.4660
Specialty
General, Plastic Surgery

Other 510(k)s with product code FZZ

510(k)DeviceApplicantDecision
K042555Surgichip Tag Surgical MarkerFZZ · Traditional Surgichip, Inc.11/09/2004SE
K915066Disposable Skin MarkerFZZ · Traditional American Medical Mfg., Inc.05/14/1992SE
K914759Bloom Transparent StencilFZZ · Traditional Freckles Publications, Inc.04/21/1992SE
K912730Rocket Surgical Skin Marking PenFZZ · Traditional West Texas Lighthouse For the Blind11/07/1991SE
K905143Skin MarkerFZZ · Traditional Aesculap, Inc.02/06/1991SE
K904559Qualtex Skin MarkerFZZ · Traditional Qualtex, Inc.12/13/1990SE
K896792Surgical Skin MarkerFZZ · Traditional Westmark, Sterile Packing Systems, Inc. (Sps)12/27/1989SE
K864371Surgical Skin MarkerFZZ · Traditional Myocure, Inc.11/17/1986SE
K863280DermamarkerFZZ · Traditional Dermacare Products, Inc.09/09/1986SE
K861772Laser Skin Marker and Mask White LotionFZZ · Traditional Pacific Poly Crafts05/21/1986SE

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Questions and answers

When was Scanlan Colormark Skin Marker cleared by the FDA?

Scanlan Colormark Skin Marker (K841085) received a 510(k) decision of Substantially Equivalent on June 11, 1984, 90 days after the submission was received.

What is the product code of K841085?

The FDA product code is FZZ – Marker, Skin, a Class I (low risk) device regulated under 21 CFR 878.4660.