Single Hair Transplant Graft

FDA 510(k) K841741 · Paris Products, Inc.

Substantially Equivalent

510(k) numberK841741

Submission

Device name
Single Hair Transplant Graft
Applicant
Paris Products, Inc.
Mchenry, IL, US
Received
April 23, 1984
Decision date
July 23, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FZT – Cutter, Surgical
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code FZT

510(k)DeviceApplicantDecision
K112400SmartshearsFZT · Traditional Nuscience Consulting and Management Group, LLC09/12/2011SE
K890818Auto Suture Disposable Surgical Trocar*FZT · Traditional United States Surgical, A Division of Tyco Healthc05/04/1989SE
K872990Micrins Surgical ScissorFZT · Traditional Micrins Surgical, Inc.08/17/1987SE
K841247SPC Disposable CutterFZT · Traditional Surgical Products Corp.05/02/1984SE
K822448Scissors, VariousFZT · Traditional J. Sklar Mfg. Co., Inc.09/14/1982SE
K821632Surgical Scissors, Set of 3FZT · Traditional Fred Sammons, Inc.06/24/1982SE
K821361Conphar Tonsil ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE
K821355Conphar Littauer ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE
K821352Conphar Iris ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE
K821351Conphar Dissecting ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE

Questions and answers

When was Single Hair Transplant Graft cleared by the FDA?

Single Hair Transplant Graft (K841741) received a 510(k) decision of Substantially Equivalent on July 23, 1984, 91 days after the submission was received.

What is the product code of K841741?

The FDA product code is FZT – Cutter, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4800.