Surgimat
FDA 510(k) K926259 · W.O.M. World of Medicine GmbH
510(k) numberK926259
Submission
- Device name
- Surgimat
- Applicant
- W.O.M. World of Medicine GmbH
Tucson, AR, US - Received
- December 18, 1992
- Decision date
- September 14, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HET – Laparoscope, Gynecologic (And Accessories)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.1720
- Specialty
- Obstetrics/Gynecology
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| K250939 | SIRIUS Endoscope System (PR-SI-1230)HET · Traditional | Precision Robotics (Hong Kong) Limited | 08/29/2025SE |
| K243821 | i-CutHET · Traditional | A.M.I. Agency For Medical Innovations GmbH | 04/25/2025SE |
| K221642 | SIRIUS Endoscope SystemHET · Traditional | Precision Robotics (Hong Kong) Limited | 12/12/2022SE |
| K210116 | Video Endoscopy System, 3D Video Endoscopy SystemHET · Traditional | Surgnova Healthcare Technologies (Zhejiang) Co.… | 10/13/2021SE |
| K201832 | Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5HET · Traditional | Olympus Medical Systems Corp. | 09/17/2021SE |
| K210104 | SurroundScope SystemHET · Traditional | 270surgical , Ltd. | 07/08/2021SE |
| K201617 | TipVision Videoscope System (TipVision VideoScope 0°/30°; EleVision HD 2 Camera Control…HET · Traditional | Schoelly Fiberoptic GmbH | 03/12/2021SE |
| K200216 | 4K UHD Camera SystemHET · Traditional | Scivita Medical Technology Co., Ltd. | 08/21/2020SE |
| K200638 | LAP-iX Suction IrrigationHET · Special | Sejong Medical Co., Ltd. | 04/03/2020SE |
| K190190 | WV1 EndoscopeHET · Traditional | 270surgical , Ltd. | 11/01/2019SE |
More from 270surgical , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K250795 | Purevue FMSHRX · Traditional | 12/05/2025SE |
| K201361 | PneumoclearHIF · Traditional | 07/29/2020SE |
| K173311 | ARTHRO-Pump PA304HRX · Traditional | 05/09/2018SE |
| K173489 | GYN-Pump PH304HIG · Traditional | 03/28/2018SE |
| K172040 | Aquilex Fluid Control System AQL-100SHIG · Special | 02/05/2018SE |
| K170784 | PneumoclearHIF · Traditional | 05/15/2017SE |
| K163320 | LAP-Pump PP110HET · Traditional | 03/21/2017SE |
| K153513 | Insufflator 50L FM134HIF · Traditional | 03/04/2016SE |
| K152109 | HD-Camera HDC1000FET · Traditional | 10/13/2015SE |
| K123732 | Hysteroscopy Pump HM6HIG · Special | 04/04/2013SE |
Questions and answers
When was Surgimat cleared by the FDA?
Surgimat (K926259) received a 510(k) decision of Substantially Equivalent on September 14, 1994, 635 days after the submission was received.
What is the product code of K926259?
The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.