Company ยท US
Broadwest Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1987. 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 |
|---|---|---|---|
| Feb 4, 1987 | K864569 | PODODIGITAL Broadwest Corp. | IKE |
| Feb 4, 1987 | K864499 | PODOSCOPE Broadwest Corp. | IKE |
| Jul 2, 1985 | K852302 | INOX IORCEPS JAR Broadwest Corp. | |
| Jul 1, 1985 | K852301 | INOX THERMOMETER JAR Broadwest Corp. | FLK |
| Jun 20, 1985 | K852300 | INOX IV STAND Broadwest Corp. | FOX |
| May 9, 1985 | K851307 | INOX DRY HEAT STERILIZER Broadwest Corp. | KMH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||