Product code JOT— General, Plastic Surgery
R2 ELECTROSURG. RETURN ELECT. #225ETC.
- Classification name
- Electrode, Gel, Electrosurgical
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 9
- First cleared
- Most recent
Market context for product code JOT
FDA has cleared devices under product code JOT between 1980 and 1992, filed by 9 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1992
- 1991
- 1990
- 1989
- 1987
- 1980
Top applicants under product code JOT
Recent clearances under product code JOT
- K923647 — RFG-DGP DISPOSABLE GROUNDING PADS
- K905545 — ULTRASOUND TRANSMISSION GEL
- K904418 — ULTRASOUND COUPLING GEL
- K901217 — TRIA-SONIC ULTRA SOUND TRANSMISSION GEL
- K894490 — STERILE ULTRASOUND TRANSMISSION GEL
- K884503 — ULTRASONIC TRANSMISSION GEL
- K872519 — STERILIZED OMNI GEL
- K871565 — ULTRASOUND TRANSDUCER GEL, STERILE
- K800933 — R2 ELECTROSURG. RETURN ELECT. #225ETC.
Data sourced from openFDA. This site is unofficial and independent of the FDA.