Product code JFC— Physical Medicine
2P-QDA FOOT PRESSURE SYSTEMS REAL TIME
- Classification name
- System, Pressure Measurement, Intermittent
- Device class
- Class 1
- Regulation
- 21 CFR 890.1600
- Advisory panel
- Physical Medicine
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code JFC
FDA has cleared devices under product code JFC between 1983 and 1993, filed by 10 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1993
- 1992
- 1991
- 1988
- 1986
- 1983
Top applicants under product code JFC
Recent clearances under product code JFC
- K924705 — FORCE SENSING ARRAY
- K925052 — QA PRESSURE MEASUREMENT SYSTEM
- K925258 — DYNAMIC PRESSURE MONITOR 2000M AND 2000C
- K915278 — CDG GAIT ANALYSES SYSTEM
- K914776 — OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITOR
- K913510 — MECHANICAL SHAPE SENSOR
- K881284 — COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE
- K882139 — 2P-QDA FOOT PRESSURE SYSTEMS REAL TIME
- K861260 — PEDABAROGRAPH
- K831800 — TEXAS INTERFACE PRESSURE EVALUATOR-TIPE
- K823681 — MODEL ICPM & ACCESSORIES
Data sourced from openFDA. This site is unofficial and independent of the FDA.