The following data is part of a premarket notification filed by Advanced Medical Technology Ltd. with the FDA for Venometer.
Device ID | K983900 |
510k Number | K983900 |
Device Name: | VENOMETER |
Classification | Plethysmograph, Photoelectric, Pneumatic Or Hydraulic |
Applicant | ADVANCED MEDICAL TECHNOLOGY LTD. 9712 S. ALTAMONT DR. Sandy, UT |
Contact | William E Mckay |
Correspondent | William E Mckay ADVANCED MEDICAL TECHNOLOGY LTD. 9712 S. ALTAMONT DR. Sandy, UT |
Product Code | JOM |
CFR Regulation Number | 870.2780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-11-03 |
Decision Date | 1999-01-29 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VENOMETER 76194685 2669965 Dead/Cancelled |
Amtec Medical Limited 2001-01-16 |
VENOMETER 72333893 0893806 Dead/Expired |
H. W. ANDERSEN PRODUCTS, INC. 1969-07-30 |
VENOMETER 72183873 0812331 Dead/Expired |
H. W. ANDERSEN PRODUCTS, INC. 1964-01-02 |