Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series

FDA 510(k) K062968 · Medsys, S.A.

Substantially Equivalent

510(k) numberK062968

Submission

Device name
Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series
Applicant
Medsys, S.A.
Puyallup, WA, US
Received
September 29, 2006
Decision date
January 3, 2007
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary 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).

Other 510(k)s with product code GCJ

510(k)DeviceApplicantDecision
K262397CuratOR EX2742GCJ · Traditional Eizo Corporation09/11/2026SE
K260884UNIDRIVE Select SystemGCJ · Traditional Karl Storz SE & CO. KG09/01/2026SE
K260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorGCJ · Traditional Sony Corporation08/26/2026SE
K261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)GCJ · Traditional Freyja Healthcare, LLC08/13/2026SE
K253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ…GCJ · Traditional Medical Impact07/24/2026SE
K261614LED LCD Monitor (OEV-271H)GCJ · Traditional Lg Electronics.Inc07/17/2026SE
K261249Universal Seal (5-12 mm)GCJ · Traditional Intuitive Surgical, Inc.07/14/2026SE
K260710FloShield Air System (FSS-01-1000T - 10mm, 0 Degree FloShield Air, FSS-02-1030T - 10mm…GCJ · Traditional FloShield, Inc.06/11/2026SE
K260414“Tech-Image” Video Endoscope SystemGCJ · Traditional Tech-Image CO., LTD.06/10/2026SE
K253994TroKit Laparoscope Lens WiperGCJ · Traditional TroCare, LLC06/04/2026SE

More from TroCare, LLC

510(k)DeviceDecision
K092897Lap LoopKNF · Traditional 02/01/2010SE
K023735Lapman Laparoscope Manipulator System and Accessories, Model 900-001GCJ · Abbreviated 08/07/2003SE

Questions and answers

When was Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series cleared by the FDA?

Lapman Laparoscope Manipulator and Accessories, Model 900-200 Series (K062968) received a 510(k) decision of Substantially Equivalent on January 3, 2007, 96 days after the submission was received.

What is the product code of K062968?

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