Suture Cutter

FDA 510(k) K780574 · Laschal Instrument Corp.

Substantially Equivalent

510(k) numberK780574

Submission

Device name
Suture Cutter
Applicant
Laschal Instrument Corp.
Mchenry, IL, US
Received
April 10, 1978
Decision date
July 17, 1978
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

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K872990Micrins Surgical ScissorFZT · Traditional Micrins Surgical, Inc.08/17/1987SE
K841741Single Hair Transplant GraftFZT · Traditional Paris Products, Inc.07/23/1984SE
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

More from Conphar, Inc.

510(k)DeviceDecision
K780575Laschal ScissorFZT · Traditional 04/18/1978SE

Questions and answers

When was Suture Cutter cleared by the FDA?

Suture Cutter (K780574) received a 510(k) decision of Substantially Equivalent on July 17, 1978, 98 days after the submission was received.

What is the product code of K780574?

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