T-Rx Retrieval Forceps
510(k) K970982
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK970982 | Date9 May 1997 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- OCZ
- Device Class
- Class II
- Regulation
- 21 CFR Part 876.1500
- Advisory Committee
- Gastroenterology, Urology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 1 Oct 2026
The T-Rx Retrieval Forceps is an Endoscopic Grasping/Cutting Instrument, Non-Powered, used in Gastroenterology and Urology. It is a medical device designed for grasping and cutting during endoscopic procedures.
The T-Rx Retrieval Forceps is supplied with FDA 510K authorizations and is classified under regulation number 876.1500. It has a product code of OCZ and is manufactured by Tri-Med Specialties, Inc.
Other devices from Tri-Med Specialties, Inc.
Questions
AI-generated answers, 1 Oct 2026
What is the T-Rx Retrieval Forceps used for?
The T-Rx Retrieval Forceps is used for grasping and cutting during endoscopic procedures in Gastroenterology and Urology.
Is the T-Rx Retrieval Forceps supplied sterile?
The description does not specify if the T-Rx Retrieval Forceps is supplied sterile, but it is classified as a non-powered endoscopic grasping/cutting instrument.
What is the regulatory classification of the T-Rx Retrieval Forceps?
The T-Rx Retrieval Forceps is classified under regulation number 876.1500 with a product code of OCZ.