The following data is part of a premarket notification filed by Access Bio Incorporate with the FDA for Carestart Hcg Combo One-step Pregnancy Test And Carestart Plus Hcg Combo One-step Pregnancy Test.
Device ID | K031048 |
510k Number | K031048 |
Device Name: | CARESTART HCG COMBO ONE-STEP PREGNANCY TEST AND CARESTART PLUS HCG COMBO ONE-STEP PREGNANCY TEST |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | ACCESS BIO INCORPORATE 675 US HIGHWAY 1 North Brunswick, NJ 08902 |
Contact | Young Ho Choi |
Correspondent | Young Ho Choi ACCESS BIO INCORPORATE 675 US HIGHWAY 1 North Brunswick, NJ 08902 |
Product Code | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-04-02 |
Decision Date | 2003-06-16 |