The following data is part of a premarket notification filed by Bio-research Associates, Inc. with the FDA for Bio-emg Model 800.
Device ID | K873947 |
510k Number | K873947 |
Device Name: | BIO-EMG MODEL 800 |
Classification | Device, Muscle Monitoring |
Applicant | BIO-RESEARCH ASSOCIATES, INC. 4113 NORTH PORT WASHINGTON RD. Milwaukee, WI 53212 |
Contact | John C Radke |
Correspondent | John C Radke BIO-RESEARCH ASSOCIATES, INC. 4113 NORTH PORT WASHINGTON RD. Milwaukee, WI 53212 |
Product Code | KZM |
CFR Regulation Number | 890.1375 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-28 |
Decision Date | 1988-04-27 |