Fallopian Tube Forceps
510(k) K810483
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK810483 | Date11 Mar 1981 | StatusActive |
Recalls
No FDA recalls found in the data synced 6 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- KNA
- Device Class
- Class II
- Regulation
- 21 CFR Part 884.4530
- Advisory Committee
- Obstetrics/Gynecology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 19 Sep 2026
The Fallopian Tube Forceps is a Manual, Specialized Obstetric-Gynecologic Instrument designed for precise grasping and manipulation of fallopian tube tissue during surgical procedures. Classified as a Class II device, it is intended for use in minimally invasive and open gynecological surgeries, including tubal ligation or other fallopian tube interventions.
Supplied as a reusable surgical tool, the device is intended for single-patient use per sterile packaging. Models such as the LA1354F feature a 5mm x 33cm shaft with a ratchet mechanism and flush port, with an overall length of 8-1/8
Other devices from American V. Mueller
Questions
AI-generated answers, 19 Sep 2026
What surgical procedures is this Fallopian Tube Forceps designed to assist with, and how does it differ from standard forceps?
The Fallopian Tube Forceps is specifically designed for precise grasping and manipulation of fallopian tube tissue during gynecological surgeries, such as tubal ligation or other fallopian tube interventions. Unlike standard forceps, it features specialized design elements like a ratchet mechanism and a flush port, which enhance control and stability when working with delicate fallopian tube tissue. It is intended for use in both minimally invasive and open surgical procedures.
Is this device reusable or single-use, and how is it packaged for sterility?
The Fallopian Tube Forceps is a reusable surgical tool, but it is supplied in sterile packaging intended for single-patient use. This ensures that each patient receives a clean and sterile instrument, reducing the risk of infection while allowing for proper reprocessing between uses in a clinical setting.
What are the key dimensions and features of the LA1354F model, and how does the shaft length compare to other models?
The LA1354F model features a shaft measuring 5mm in width by 33cm in length, with an overall length of 8-1/8 inches. This design provides a balance of precision and reach for delicate fallopian tube procedures. While the exact dimensions of other models aren’t specified, the shaft length and width are tailored to facilitate controlled manipulation during gynecological surgeries.
How should this device be stored to maintain its integrity and sterility?
Since the Fallopian Tube Forceps is reusable and supplied in sterile packaging for single-patient use, it should be stored in a clean, dry environment away from direct sunlight or extreme temperatures. After use, it must undergo proper reprocessing (cleaning, disinfection, and sterilization) before storage to ensure sterility for subsequent procedures. Always follow manufacturer guidelines for storage and reprocessing.