Radionics Single Use Ground Pad (Dgp-Hp)

K030697 is the FDA 510(k) clearance record for RADIONICS SINGLE USE GROUND PAD (DGP-HP), a class II device, cleared for Radionics, Inc. on 2003-04-04 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 57 510(k) clearances for Radionics, Inc., from 1982-07-22 to 2012-02-22. As of 2026-09-10, FDA records show one recall naming K030697.