Home › Macan Manufacturing › Macan
Macan
Macan Manufacturing · Model UF-L40 · UDI-DI 00851708006142
1
510(k) clearances
13
Adverse events
1
Recalls
9
Facilities
Description
UF-L40 Electrode (2 pk)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-04-05 | Macan Engineering and Manufacturing Co., Inc. | The product label fails to warn users to use the device on patients with shielded pacemakers only. |
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.
