Marlow Laparoscopic Scissors

FDA 510(k) K914869 · Marlo Surgical Technology

Substantially Equivalent

510(k) numberK914869

Submission

Device name
Marlow Laparoscopic Scissors
Applicant
Marlo Surgical Technology
Willoughby, OH, US
Received
October 29, 1991
Decision date
January 15, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from TroCare, LLC

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K932634Nu-Tip(Tm) Forceps:Graspers/Dissectors/SuturesHET · Traditional 02/25/1994SE
K920611Marlow Laparoscopic Grasping ForcepGCJ · Traditional 04/20/1993SE
K914153Ott Insufflator Filter Plus/Tubing SetHIF · Traditional 04/02/1992SE
K913954Marlow/Reddick Laparoscopic Needle HoldersGCJ · Traditional 12/18/1991SE
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K913964Marlow/Reddick Laparoscopic Grasping ForcepsHTD · Traditional 10/23/1991SE

Questions and answers

When was Marlow Laparoscopic Scissors cleared by the FDA?

Marlow Laparoscopic Scissors (K914869) received a 510(k) decision of Substantially Equivalent on January 15, 1992, 78 days after the submission was received.

What is the product code of K914869?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.