JOT
9 FDA 510(k) clearances · Product code
101 daysmedian time to decision
137 days90th percentile
9clearances measured
FDA profile
- Official device name
- Electrode, Gel, Electrosurgical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Medical specialty
- General, Plastic Surgery
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| RFG-DGP DISPOSABLE GROUNDING PADS (K923647) | Radionics, Inc. | 1992-11-09 |
| ULTRASOUND TRANSMISSION GEL (K905545) | Arbo Medical, Inc. | 1991-03-29 |
| ULTRASOUND COUPLING GEL (K904418) | Geno Laboratories | 1991-02-11 |
| TRIA-SONIC ULTRA SOUND TRANSMISSION GEL (K901217) | H & P Industries, Inc. | 1990-06-22 |
| STERILE ULTRASOUND TRANSMISSION GEL (K894490) | Swedish Trade Council USA | 1989-10-05 |
| ULTRASONIC TRANSMISSION GEL (K884503) | Herbert Stanley Co. | 1989-02-13 |
| STERILIZED OMNI GEL (K872519) | Echo Ultrasound | 1987-08-03 |
| ULTRASOUND TRANSDUCER GEL, STERILE (K871565) | Amedic USA | 1987-07-15 |
| R2 ELECTROSURG. RETURN ELECT. #225ETC. (K800933) | R2 Corp. | 1980-05-20 |
Track JOT automatically
Every clearance here is in the API, with alerts when new ones post.