Meditech is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meditech - FDA 510(k) Cleared Devices
Recent clearances: NIDA-5/RT, DRUG OF ABUSE CONTROLS
1
Total
1
Cleared
0
Denied
Meditech, is a healthcare software and EHR platform company with a manufacturing facility in Ventura, US. The company develops electronic health record systems and clinical decision support solutions for healthcare organizations.
Meditech has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory history focuses on Toxicology devices, with its cleared device being the NIDA-5/RT Drug of Abuse Controls. The company's first and latest FDA 510(k) clearance dates to 1994.
Meditech is currently inactive in terms of FDA 510(k) submissions, with no new clearances in more than five years. This regulatory record represents a historical snapshot of the company's medical device portfolio. For detailed information on device names, product codes, and clearance dates, consult the FDA's 510(k) database.
FDA 510(k) Regulatory Record - Meditech
1 devices