Coopersurgical Malleable Sytlet
FDA 510(k) K023382 · Cooper Surgical
510(k) numberK023382
Submission
- Device name
- Coopersurgical Malleable Sytlet
- Applicant
- Cooper Surgical
Huntington, CT, US - Received
- October 8, 2002
- Decision date
- December 20, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MQF – Catheter, Assisted Reproduction
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.6110
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code MQF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253354 | Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C…MQF · Traditional | Guangzhou Hehong Biotech Co., Ltd. | 02/12/2026SE |
| K243373 | Embryo Transfer Catheter (ETC) Assortment: EmbryoCath Embryo Transfer Catheter -…MQF · Traditional | Vitrolife Sweden AB | 07/23/2025SE |
| K240307 | VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)MQF · Traditional | Shenzhen Vitavitro Biotech Co., Ltd. | 08/16/2024SE |
| K231730 | FemaSeed Intratubal InseminationMQF · Traditional | Femasys, Inc. | 09/22/2023SE |
| K220010 | Daylily Single Use Sterile Embryo Transfer CatheterMQF · Traditional | Shanghai Horizon Medical Technology Co., Ltd. | 12/16/2022SE |
| K200248 | Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft ObturatorsMQF · Traditional | Allwin Medical Devices, Inc. | 07/01/2020SE |
| K192540 | Kitazato ET CathetersMQF · Traditional | Kitazato Corporation | 05/01/2020SE |
| K190522 | Allwin Intra Uterine Insemination Catheters (INSEMINA and INSEMINA Open Tip Intra…MQF · Traditional | Allwin Medical Devices, Inc. | 11/14/2019SE |
| K191015 | Soft-Pass Embryo Mock Transfer Catheter Sets (Soft-Pass Embryo Mock Transfer Catheter…MQF · Special | Cook Incorporated | 05/17/2019SE |
| K180302 | Guardia Access Malleable Obturator, Guardia Obturator, Soft-Pass Obturator…MQF · Traditional | Cook Incorporated | 10/24/2018SE |
More from Cook Incorporated
| 510(k) | Device | Decision |
|---|---|---|
| K253698 | Milex Incontinence Dish Pessaries; Milex Incontinence Dish Pessaries with Support…HHW · Traditional | 01/20/2026SE |
| K091325 | Ten-Year Fracture Risk Option and Siri Table Option for Norland Dxa Bone DensitometersKGI · Traditional | 06/29/2009SE |
| K023384 | Coopersurgical Trial Transfer CatheterMQF · Traditional | 12/13/2002SE |
| K023383 | Coopersurgical Intrauterine Insemination CatheterMQF · Traditional | 12/13/2002SE |
| K023379 | Coopersurgical Embryo Transfer Catheter, Coopersurgical Assisted Reproduction CatheterMQF · Traditional | 12/11/2002SE |
Questions and answers
When was Coopersurgical Malleable Sytlet cleared by the FDA?
Coopersurgical Malleable Sytlet (K023382) received a 510(k) decision of Substantially Equivalent on December 20, 2002, 73 days after the submission was received.
What is the product code of K023382?
The FDA product code is MQF – Catheter, Assisted Reproduction, a Class II (moderate risk) device regulated under 21 CFR 884.6110.