The following data is part of a premarket notification filed by Karlin Technology, Inc. with the FDA for X-ray Marker.
Device ID | K882519 |
510k Number | K882519 |
Device Name: | X-RAY MARKER |
Classification | System, X-ray, Film Marking, Radiographic |
Applicant | KARLIN TECHNOLOGY, INC. 330 WASHINGTON ST. SUITE 314 Marina Del Rey, CA 90292 |
Contact | Mark Weidhaas |
Correspondent | Mark Weidhaas KARLIN TECHNOLOGY, INC. 330 WASHINGTON ST. SUITE 314 Marina Del Rey, CA 90292 |
Product Code | JAC |
CFR Regulation Number | 892.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-06-17 |
Decision Date | 1988-08-09 |