Rocket Surgical Skin Marking Pen

FDA 510(k) K912730 · West Texas Lighthouse For the Blind

Substantially Equivalent

510(k) numberK912730

Submission

Device name
Rocket Surgical Skin Marking Pen
Applicant
West Texas Lighthouse For the Blind
San Angelo, TX, US
Received
June 20, 1991
Decision date
November 7, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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
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
K844865Securline Surgical Skin Marker 1000FZZ · Traditional Precision Dynamics Corp.01/14/1985SE

Questions and answers

When was Rocket Surgical Skin Marking Pen cleared by the FDA?

Rocket Surgical Skin Marking Pen (K912730) received a 510(k) decision of Substantially Equivalent on November 7, 1991, 140 days after the submission was received.

What is the product code of K912730?

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