The following data is part of a premarket notification filed by Consolidated Medical Equipment, Inc. with the FDA for Disposable Conductive Adhesive Diagnostic Ecg Elec.
Device ID | K850132 |
510k Number | K850132 |
Device Name: | DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELEC |
Classification | Electrode, Electrocardiograph |
Applicant | CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
Contact | William W Abraham |
Correspondent | William W Abraham CONSOLIDATED MEDICAL EQUIPMENT, INC. 310 BROAD ST. Utica, NY 13501 |
Product Code | DRX |
CFR Regulation Number | 870.2360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-01-14 |
Decision Date | 1985-04-09 |