The following data is part of a premarket notification filed by Impac Medical Systems, Inc. with the FDA for Sequencer.
Device ID | K913612 |
510k Number | K913612 |
Device Name: | SEQUENCER |
Classification | Accelerator, Linear, Medical |
Applicant | IMPAC MEDICAL SYSTEMS, INC. 182 UNIVERSITY AVE. Palo Alto, CA 94301 |
Contact | Joseph Jachinowski |
Correspondent | Joseph Jachinowski IMPAC MEDICAL SYSTEMS, INC. 182 UNIVERSITY AVE. Palo Alto, CA 94301 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-14 |
Decision Date | 1991-12-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SEQUENCER 90763916 not registered Live/Pending |
Axis Group, LLC 2021-06-09 |
SEQUENCER 75197286 not registered Dead/Abandoned |
Studio e, Inc. 1996-11-13 |
SEQUENCER 75197285 not registered Dead/Abandoned |
Studio e, Inc. 1996-11-13 |