Doctor'S Research Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE, DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00, LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
13
Total
13
Cleared
0
Denied
FDA 510(k) Regulatory Record - Doctor'S Research Group, Inc. Ear, Nose, Throat ✕
1 devices