Home › HUESTIS MACHINE CORPORATION › Huestis Medical Collimator
Huestis Medical Collimator
HUESTIS MACHINE CORPORATION · Model CM-3201-008 · UDI-DI 00850077007019
1
510(k) clearances
5
Adverse events
4
Recalls
13
Facilities
Description
Collimator FRU for Definium 5000, (Huestis Part # CM-3201-008), (GEHC Part # 5212898), (GE # 6693-50GE), (GE Catalog # B1100SL)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-10-28 | Shimadzu Medical Systems | Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray system and Diagnostic x-ray tube assembly because they do not comply with the Product Performance Standard |
| 2007-08-10 | Summit Industries Inc. | The D800 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |
| 2007-08-10 | Summit Industries Inc. | The E600 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |
| 2007-08-10 | Summit Industries Inc. | The F100 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table. |
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.
