Product code ITJ— Physical Medicine
WALKING AID
- Classification name
- Walker, Mechanical
- Device class
- Class 1
- Regulation
- 21 CFR 890.3825
- Advisory panel
- Physical Medicine
- Total cleared
- 14
- First cleared
- Most recent
Market context for product code ITJ
FDA has cleared devices under product code ITJ between 1977 and 1983, filed by 13 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
- 1983
- 1982
- 1981
- 1979
- 1977
Top applicants under product code ITJ
Adverse events under product code ITJ
product code ITJ- Death
- 8
- Injury
- 571
- Other
- 2
- Total
- 581
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code ITJ
- K833869 — CHILD'S WALKER
- K833195 — UMBRELLA WALKER
- K830784 — WALK N ROLL
- K830848 — RESI-WALKER
- K823105 — RESI-WALKER
- K821404 — LIGHT WEIGHT ALUMINUM WALKER
- K820711 — WALK-A-CYCLE
- K811485 — WALKER/CRUTCH BAG
- K792064 — DELTA ROLLING SELF-LICKING WALKER
- K790529 — WALKING AID
- K772049 — WALKING AID
- K770417 — ANIMATOR
- K770608 — WALKING AID
- K770166 — MANOY WALKING AID
Data sourced from openFDA. This site is unofficial and independent of the FDA.