Home › HANS RUDOLPH, INC. › N/A
N/A
HANS RUDOLPH, INC. · Model 8410 · UDI-DI 00874750006809
JAX
Prescription
8
510(k) clearances
2
Adverse events
1
Recalls
4
Facilities
Description
HTR SHELL/CABLE ASSY REF8410
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-09 | Philips Medical Systems (Cleveland) Inc | When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.