The following data is part of a premarket notification filed by Electromedics, Inc. with the FDA for Bt-795/ats.
Device ID | K871847 |
510k Number | K871847 |
Device Name: | BT-795/ATS |
Classification | Apparatus, Autotransfusion |
Applicant | ELECTROMEDICS, INC. P.O. BOX 3315 Englewood, CO 80155 |
Contact | Dennis Mcelwee |
Correspondent | Dennis Mcelwee ELECTROMEDICS, INC. P.O. BOX 3315 Englewood, CO 80155 |
Product Code | CAC |
CFR Regulation Number | 868.5830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-05-12 |
Decision Date | 1987-06-19 |