Dexide Laparoscopic Accessories
FDA 510(k) K923845 · Dexide, Inc.
510(k) numberK923845
Submission
- Device name
- Dexide Laparoscopic Accessories
- Applicant
- Dexide, Inc.
Fort Worth, TX, US - Received
- July 31, 1992
- Decision date
- November 25, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GEI – Electrosurgical, Cutting & Coagulation & Accessories
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Specialty
- General, Plastic Surgery
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 GEI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254185 | Potenza PrimeGEI · Traditional | Jeisys Medical Incorporated | 09/11/2026SE |
| K262364 | Ellian Enigma RF DeviceGEI · Traditional | Ellian Corp | 09/02/2026SE |
| K253859 | Scarlet Pro (Scarlet Pro)GEI · Traditional | VIOL Co., Ltd. | 08/27/2026SE |
| K252535 | Inno-Switch Laparoscopic InstrumentsGEI · Traditional | Taiwan Surgical Corporation | 08/25/2026SE |
| K261179 | AlphaTriPart - Monopolar MIC InstrumentsGEI · Traditional | Gimmi GmbH | 07/22/2026SE |
| K253504 | VolnewmerGEI · Traditional | Classys, Inc. | 07/13/2026SE |
| K254056 | THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35…GEI · Traditional | Olympus Medical Systems Corp. | 07/01/2026SE |
| K253484 | Lutronic GeniusGEI · Traditional | Cynosure Lutronic Technology Corporation | 06/29/2026SE |
| K251492 | Irrigation Tubing Bipolar Cord SetGEI · Traditional | New Deantronics Taiwan , Ltd. | 06/29/2026SE |
| K260636 | Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingGEI · Traditional | Stryker Sustainability Solutions | 06/18/2026SE |
More from Stryker Sustainability Solutions
| 510(k) | Device | Decision |
|---|---|---|
| K991814 | Multachoice InstrumentsGEI · Special | 06/23/1999SE |
| K990379 | Modification to Multaport Cannula, Reducer and AccessoriesGCJ · Special | 03/04/1999SE |
| K981940 | Multapump Disposable Pump Head and AccessoriesGCJ · Traditional | 09/25/1998SE |
| K981941 | Multaport Cannula Reducer and AccessoriesGCJ · Traditional | 07/29/1998SE |
| K953611 | Dexide Endo-Lube KitGCJ · Traditional | 09/15/1995SE |
| K944509 | Dexide Insufflation Tubing with FilterHIF · Traditional | 02/07/1995SE |
| K924117 | Dexide Laparoscopic KitsKDD · Traditional | 03/23/1993SESK |
| K921709 | Endobag, ModificationGCJ · Traditional | 07/14/1992SE |
| K913762 | Monoscopy(Tm) Brand, EndobagGCJ · Traditional | 10/28/1991SE |
| K912637 | Laparoscopic Electrosurgical Cannula W/RetractableGEI · Traditional | 10/04/1991SE |
Questions and answers
When was Dexide Laparoscopic Accessories cleared by the FDA?
Dexide Laparoscopic Accessories (K923845) received a 510(k) decision of Substantially Equivalent on November 25, 1992, 117 days after the submission was received.
What is the product code of K923845?
The FDA product code is GEI – Electrosurgical, Cutting & Coagulation & Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4400.