Deltaglide is one of 25877 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Deltaglide has 1 FDA 510(k) cleared medical devices. Based in Hamden, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Deltaglide Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Deltaglide
1 devices