Ge Healthcare Coils (Usa Instruments, Inc.)
Ge Healthcare Coils (Usa Instruments, Inc.) appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 23, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253738 | 3.0T AIR 32CH HNA | January 23, 2026 |
| K223378 | 3.0T 16ch AIR AA | January 3, 2023 |
| K182504 | 3.0T Air MP M, 3.0T Air MP L | October 12, 2018 |
| K180666 | 48CH Head Coil | April 12, 2018 |
| K172695 | AIR Anterior Array, AIR Posterior Array | November 22, 2017 |
| K163205 | 48CH Head Coil | January 12, 2017 |
| K143389 | 3.0T GEM RT Open Array | March 6, 2015 |
| K123327 | 1.5T GEM RT OPEN ARRAY | January 11, 2013 |
| K122174 | PEDIATRIC POSITIONER PAD SET | November 16, 2012 |
| K103365 | DISCOVERY 3T 16 CH BODY ARRAY COIL (ANTERIOR); DISCOVERY 3T 16 CH BODY ARRAY COIL (POSTERIOR); DISCO | January 12, 2011 |
| K101492 | 8 CHANNEL CARDIAC PHASED ARRAY COIL | June 23, 2010 |
| K093348 | 3.0T 16 CHANNEL HEAD NECK SPINE COIL | November 25, 2009 |