The following data is part of a premarket notification filed by Lifescan, Inc. with the FDA for One Touch Ii Hospital Blood Glucose Monitoring System Data Dock.
Device ID | K972473 |
510k Number | K972473 |
Device Name: | ONE TOUCH II HOSPITAL BLOOD GLUCOSE MONITORING SYSTEM DATA DOCK |
Classification | Glucose Oxidase, Glucose |
Applicant | LIFESCAN, INC. 1000 GIBRALTAR DR. Milpitas, CA 95035 -6312 |
Contact | John E Hughes |
Correspondent | John E Hughes LIFESCAN, INC. 1000 GIBRALTAR DR. Milpitas, CA 95035 -6312 |
Product Code | CGA |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-07-01 |
Decision Date | 1997-12-16 |
Summary: | summary |