Endo I/A Probe
FDA 510(k) K924149 · Snowden-Pencer
510(k) numberK924149
Submission
- Device name
- Endo I/A Probe
- Applicant
- Snowden-Pencer
Tucker, GA, US - Received
- August 18, 1992
- Decision date
- January 26, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K262397 | CuratOR EX2742GCJ · Traditional | Eizo Corporation | 09/11/2026SE |
| K260884 | UNIDRIVE Select SystemGCJ · Traditional | Karl Storz SE & CO. KG | 09/01/2026SE |
| K260972 | OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorGCJ · Traditional | Sony Corporation | 08/26/2026SE |
| K261139 | VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)GCJ · Traditional | Freyja Healthcare, LLC | 08/13/2026SE |
| K253541 | EZ-Close (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ…GCJ · Traditional | Medical Impact | 07/24/2026SE |
| K261614 | LED LCD Monitor (OEV-271H)GCJ · Traditional | Lg Electronics.Inc | 07/17/2026SE |
| K261249 | Universal Seal (5-12 mm)GCJ · Traditional | Intuitive Surgical, Inc. | 07/14/2026SE |
| K260710 | FloShield 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 |
| K253994 | TroKit Laparoscope Lens WiperGCJ · Traditional | TroCare, LLC | 06/04/2026SE |
More from TroCare, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K030890 | SwitchbladeGEI · Traditional | 04/04/2003SE |
| K960400 | Diamond-Touch and Micro Diamond-Touch Instruments/Diamond-Line…FBM · Traditional | 03/12/1996SE |
| K930666 | Reusable Laparoscopic Instruments W/ ElectrocauteryGEI · Traditional | 05/19/1994SE |
| K930667 | Reusable Laparoscopic InstrumentsGCJ · Traditional | 05/16/1994SE |
| K924148 | Diamond-Sharp(R) TrocarsHFI · Traditional | 02/28/1994SE |
| K920985 | Snowden-Pencer Irrigation PumpHEI · Traditional | 06/09/1992SE |
| K920986 | Snowden-Pencer High Flow Insufflator, SP/88-9700HIF · Traditional | 06/04/1992SE |
| K913979 | Endo I/A Y SetHIF · Traditional | 11/27/1991SE |
| K913835 | Snowden-Pencer Insufflator Tubing SetHIF · Traditional | 11/07/1991SE |
| K861372 | Electrosurgical Cutting and Coagulation AccessoryGEI · Traditional | 06/19/1986SE |
Questions and answers
When was Endo I/A Probe cleared by the FDA?
Endo I/A Probe (K924149) received a 510(k) decision of Substantially Equivalent on January 26, 1993, 161 days after the submission was received.
What is the product code of K924149?
The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.