The following data is part of a premarket notification filed by B C Medical Ltd. with the FDA for Bcm-400c.
Device ID | K920862 |
510k Number | K920862 |
Device Name: | BCM-400C |
Classification | System, X-ray, Angiographic |
Applicant | B C MEDICAL LTD. 3755 RICHELIEU ST-HUBERT, QC CANADA J3y 7p9, CA |
Contact | Yvan Giard |
Correspondent | Yvan Giard B C MEDICAL LTD. 3755 RICHELIEU ST-HUBERT, QC CANADA J3y 7p9, CA |
Product Code | IZI |
CFR Regulation Number | 892.1600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-02-25 |
Decision Date | 1992-09-30 |