The following data is part of a premarket notification filed by Oakfield Instruments, Ltd. with the FDA for Sourcerer.
Device ID | K894902 |
510k Number | K894902 |
Device Name: | SOURCERER |
Classification | Counter (beta, Gamma) For Clinical Use |
Applicant | OAKFIELD INSTRUMENTS, LTD. OAKFIELD INDUSTRIAL ESTATE STANTON HARCOURT RD, EYNSHAM Oxon Ox8 1ja England, GB |
Contact | John Giddings |
Correspondent | John Giddings OAKFIELD INSTRUMENTS, LTD. OAKFIELD INDUSTRIAL ESTATE STANTON HARCOURT RD, EYNSHAM Oxon Ox8 1ja England, GB |
Product Code | JJJ |
CFR Regulation Number | 862.2320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-01 |
Decision Date | 1989-10-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SOURCERER 90023142 not registered Live/Pending |
Brain Electrophysiology Laboratory Company, LLC 2020-06-26 |
![]() SOURCERER 76685546 not registered Dead/Abandoned |
The Butman Company 2008-01-07 |
![]() SOURCERER 75486717 2313296 Live/Registered |
VEECO INSTRUMENTS INC. 1998-05-18 |
![]() SOURCERER 75128340 not registered Dead/Abandoned |
National Library of Medicine of the U.S. Department of Health and Human Services 1996-07-01 |
![]() SOURCERER 74010495 1632208 Dead/Cancelled |
ION TECH, INC. 1989-12-13 |
![]() SOURCERER 73658571 1478969 Dead/Cancelled |
SAMI/BURKE INC. 1987-05-04 |