The following data is part of a premarket notification filed by Selfcare, Inc. with the FDA for Modification To Fasttake Compact Blood Glucose Monitoring System.
Device ID | K001427 |
510k Number | K001427 |
Device Name: | MODIFICATION TO FASTTAKE COMPACT BLOOD GLUCOSE MONITORING SYSTEM |
Classification | Glucose Oxidase, Glucose |
Applicant | SELFCARE, INC. 200 PROSPECT ST. Waltham, MA 02154 -3457 |
Contact | Carol A Adiletto |
Correspondent | Carol A Adiletto SELFCARE, INC. 200 PROSPECT ST. Waltham, MA 02154 -3457 |
Product Code | CGA |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-05-05 |
Decision Date | 2000-06-02 |