The following data is part of a premarket notification filed by International Newtech Development, Inc. with the FDA for Ps-unit Cassette/serum And Urine Combo Hcg.
Device ID | K974009 |
510k Number | K974009 |
Device Name: | PS-UNIT CASSETTE/SERUM AND URINE COMBO HCG |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | INTERNATIONAL NEWTECH DEVELOPMENT, INC. 1629 FOSTERS WAY Delta, British Columbia, CA V3m 6s7 |
Contact | Benny Wang |
Correspondent | Benny Wang INTERNATIONAL NEWTECH DEVELOPMENT, INC. 1629 FOSTERS WAY Delta, British Columbia, CA V3m 6s7 |
Product Code | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-10-21 |
Decision Date | 1998-03-13 |