Company ยท US
Reimers Systems, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2011. 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
| Code | Device | Records |
|---|---|---|
| CBF | Chamber, Hyperbaric | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 19, 2011 | K102831 | RSI 4200 Reimers Systems, Inc. | CBF |
| Oct 23, 1996 | K962871 | ODS1 - HOOD DRIVER Reimers Systems, Inc. | CBF |
| Oct 23, 1996 | K962869 | GSP1 - GAS SELECTION PANEL Reimers Systems, Inc. | CBF |
| Dec 15, 1995 | K954387 | T CLASS HYPERBARIC FACILITIES Reimers Systems, Inc. | CBF |
| Jun 2, 1995 | K951125 | LIFEFORCE CLINICAL HYPERBARIC FACILITY Reimers Systems, Inc. | CBF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||