Company ยท US
Howard Instruments, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2007. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| May 16, 2007 | K063104 | FOX MEDICAL DIODE LASER SYSTEM 810NM Howard Instruments, Inc. | GEX |
| Jun 17, 2003 | K030948 | VMATE MODEL VMM1000 Howard Instruments, Inc. | HQE |
| May 1, 1998 | K980985 | SCMD-1000 Howard Instruments, Inc. | HNO |
| Apr 22, 1998 | K974598 | MICROKERATOME OR THE MATE Howard Instruments, Inc. | HNO |
| Oct 10, 1997 | K972727 | CBALK-1000 BLADE Howard Instruments, Inc. | HNO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||