The following data is part of a premarket notification filed by Imatron, Inc. with the FDA for Imatron C-100 Ultrafast Ct Scanner.
Device ID | K872615 |
510k Number | K872615 |
Device Name: | IMATRON C-100 ULTRAFAST CT SCANNER |
Classification | System, X-ray, Tomography, Computed |
Applicant | IMATRON, INC. 389 OYSTER POINT BLVD. South San Francisco, CA 94080 |
Contact | Coduto |
Correspondent | Coduto IMATRON, INC. 389 OYSTER POINT BLVD. South San Francisco, CA 94080 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-07-06 |
Decision Date | 1987-09-23 |