Product code IQM— Physical Medicine

FINGEO EXTENSION SPLINTS

Classification name: Splint, Temporary Training
Device class: Class 1
Regulation: 21 CFR 890.3025
Advisory panel: Physical Medicine
Total cleared: 3
First cleared: 1977-05-26
Most recent: 1977-07-21

Market context for product code IQM

FDA has cleared 3 devices under product code IQM, all in 1977, filed by 2 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.

Top applicants under product code IQM

Orthopedic Systems, Inc.2 clearances
Fred Sammons, Inc.1 clearance

Recent clearances under product code IQM

K771287 — FINGEO EXTENSION SPLINTSFred Sammons, Inc.·1977-07-21
K770890 — SPLINT, COCKUPOrthopedic Systems, Inc.·1977-05-26
K770891 — SPLINH, FOREARMOrthopedic Systems, Inc.·1977-05-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.