Zeta Development Laboratories is one of 25768 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zeta Development Laboratories - FDA 510(k) Cleared Devices
Recent clearances: ZETA DIAGNOSTIC RETINAL IMAGING SYSTEM
1
Total
1
Cleared
0
Denied
Zeta Development Laboratories has 1 FDA 510(k) cleared medical devices. Based in El Dorado Hills, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Zeta Development Laboratories Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zeta Development Laboratories
1 devices