Monik - Disposable Endoscopic Trocar
FDA 510(k) K233386 · M/s. Meril Endo Surgery Private Limited.
510(k) numberK233386
Submission
- Device name
- Monik - Disposable Endoscopic Trocar
- Applicant
- M/s. Meril Endo Surgery Private Limited.
Vapi, IN - Received
- October 2, 2023
- Decision date
- May 24, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary 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).
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| 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 |
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| K172149 | FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable…GAP · Special | 10/20/2017SE |
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Questions and answers
When was Monik - Disposable Endoscopic Trocar cleared by the FDA?
Monik - Disposable Endoscopic Trocar (K233386) received a 510(k) decision of Substantially Equivalent on May 24, 2024, 235 days after the submission was received.
What is the product code of K233386?
The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.