Company ยท US
Briox Technologies, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1982. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 12, 1982 | K813507 | INFALERT Briox Technologies, Inc. | BZQ |
| Feb 5, 1980 | K800078 | BRIOX MODEL-AEROMIST Briox Technologies, Inc. | |
| Jul 24, 1979 | K791241 | BRIOX MODEL 2000-CA COMPRESSOR UNIT Briox Technologies, Inc. | JCX |
| Jul 24, 1979 | K791240 | BRIOX MODEL 2000-C COMPRESSOR UNIT Briox Technologies, Inc. | JCX |
| Jul 24, 1979 | K791239 | BRIOX MODEL 2000-A ASPIRATOR UNIT Briox Technologies, Inc. | JCX |
| Jul 24, 1979 | K791238 | BRIOX MODEL 2000-CQ QUIET COMPRESSOR Briox Technologies, Inc. | JCX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||