The following data is part of a premarket notification filed by Tosoh Medics, Inc. with the FDA for Aia-pack Brca, St Aia Pack Brca.
| Device ID | K010796 |
| 510k Number | K010796 |
| Device Name: | AIA-PACK BRCA, ST AIA PACK BRCA |
| Classification | System, Test, Immunological, Antigen, Tumor |
| Applicant | TOSOH MEDICS, INC. 347 OYSTER POINT BLVD., SUITE 201 San Francisco, CA 94080 |
| Contact | Lois Nakayama |
| Correspondent | Lois Nakayama TOSOH MEDICS, INC. 347 OYSTER POINT BLVD., SUITE 201 San Francisco, CA 94080 |
| Product Code | MOI |
| CFR Regulation Number | 866.6010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-03-16 |
| Decision Date | 2001-08-16 |