Company ยท US
Holgrath Medical Technologies, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1996. 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 31, 1996 | K954835 | HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET Holgrath Medical Technologies, Inc. | CAZ |
| Jul 25, 1995 | K946047 | HOLGRATH METAL-HUB, EPIDURAL NEEDLE Holgrath Medical Technologies, Inc. | BSP |
| Jun 7, 1995 | K944908 | HOLGRATH PLASTIC-HUB, COICAL POINT SPINAL NEEDLE Holgrath Medical Technologies, Inc. | BSP |
| Jun 7, 1995 | K944907 | HOLGRATH PLASTIC-HUB, QUINCKE SPINAL NEEDLE Holgrath Medical Technologies, Inc. | BSP |
| Jun 7, 1995 | K944906 | HOLGRATH PLASTIC-HUB EPIDURAL NEEDLE Holgrath Medical Technologies, Inc. | BSP |
| Jun 7, 1995 | K944905 | HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE Holgrath Medical Technologies, Inc. | BSP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||