The following data is part of a premarket notification filed by Glaxo, Inc. with the FDA for Volumatic.
Device ID | K844169 |
510k Number | K844169 |
Device Name: | VOLUMATIC |
Classification | Bougie, Esophageal, Ent |
Applicant | GLAXO, INC. 5 MOORE DR. P.O. BOX 13358 Research Triangle, NC 27709 |
Contact | David Macfarlane |
Correspondent | David Macfarlane GLAXO, INC. 5 MOORE DR. P.O. BOX 13358 Research Triangle, NC 27709 |
Product Code | KCD |
CFR Regulation Number | 874.4420 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-10-25 |
Decision Date | 1984-11-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VOLUMATIC 87047927 not registered Dead/Abandoned |
8I LIMITED 2016-05-24 |
VOLUMATIC 76239676 2743508 Dead/Cancelled |
L'Oreal 2001-04-11 |
VOLUMATIC 74306153 1818336 Dead/Cancelled |
HELENA RUBINSTEIN, S.A. 1992-08-21 |
VOLUMATIC 72453035 1003957 Dead/Expired |
CHICAGO PNEUMATIC TOOL COMPANY 1973-03-30 |
VOLUMATIC 72446026 0981098 Dead/Expired |
ROMLA COMPANY, INC. 1973-01-15 |
VOLUMATIC 72067810 0685492 Dead/Cancelled |
MOTOROLA, INC. 1959-02-16 |
VOLUMATIC 72037880 0664049 Dead/Expired |
JAMES MFG. CO. 1957-09-26 |