Product code IKX— Physical Medicine
BATH TUB SAFETY BAR
- Classification name
- Aid, Transfer
- Device class
- Class 1
- Regulation
- 21 CFR 890.5050
- Advisory panel
- Physical Medicine
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code IKX
FDA has cleared devices under product code IKX between 1978 and 1986, filed by 8 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
- 1986
- 1984
- 1983
- 1982
- 1981
- 1979
- 1978
Top applicants under product code IKX
Adverse events under product code IKX
product code IKX- Death
- 11
- Total
- 11
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 IKX
- K862895 — TRICYCLES
- K842650 — WALL GRAB BARS 98130-98136
- K831541 — TUB TRANSFER BENCH BK6481
- K823639 — BOARD TO TRANSFER PARALYZED PATIENT FROM
- K823640 — BATH TUB SAFETY BAR
- K823634 — CHAIR OR BED LEG EXTENDERS
- K823153 — BATH TUB SEAT & BATH BOARD
- K823154 — SHOWER STOOL W/HANDLES
- K821903 — DISC-O-AID
- K821010 — BATHTUB TRANSFER BENCH
- K813629 — BK-6111 HI-D TRANSFER BOARD
- K812475 — TRANSFER BENCH
- K810449 — TRANSFER AIDS
- K810275 — GRAB BARS
- K792247 — TAYLOR PATIENT TRANSFER BOARD
- K781201 — BOARD, TRANSFER, FENDER
- K780935 — GRAB BAR
- K772417 — SLIDING BOARD
Data sourced from openFDA. This site is unofficial and independent of the FDA.