Company ยท US
Howtek, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 2002. 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 |
|---|---|---|---|
| Aug 12, 2002 | K021949 | FULCRUM Howtek, Inc. | LMA |
| Nov 5, 1997 | K973081 | DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0) Howtek, Inc. | LLZ |
| Sep 8, 1997 | K972191 | DIGITIZER DIRECTOR (HSC025-01) Howtek, Inc. | LMD |
| May 20, 1997 | K970908 | HOWTEK 960 Howtek, Inc. | LMA |
| Jan 18, 1996 | K953117 | SCANMASTER DX Howtek, Inc. | LMA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||