The following data is part of a premarket notification filed by Beckman Coulter, Inc. with the FDA for Access Total Bhcg.
Device ID | K023480 |
510k Number | K023480 |
Device Name: | ACCESS TOTAL BHCG |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | BECKMAN COULTER, INC. 1000 LAKE HAZELTINE DR. Chaska, MN 55318 -1084 |
Contact | Denise Thompson |
Correspondent | Denise Thompson BECKMAN COULTER, INC. 1000 LAKE HAZELTINE DR. Chaska, MN 55318 -1084 |
Product Code | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-10-17 |
Decision Date | 2002-12-20 |
Summary: | summary |