The following data is part of a premarket notification filed by Polymedco, Inc. with the FDA for Poly-chem Glucose.
Device ID | K020852 |
510k Number | K020852 |
Device Name: | POLY-CHEM GLUCOSE |
Classification | Hexokinase, Glucose |
Applicant | POLYMEDCO, INC. 510 FURNACE DOCK RD. Cortlandt Manor, NY 10567 |
Contact | Helen Landicho |
Correspondent | Cindy Williams POLYMEDCO, INC. 5449 Reseach Drive Canton, MI 48188 |
Product Code | CFR |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-03-15 |
Decision Date | 2002-07-03 |