Company ยท US
Perimed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2016. Name variants (Inc, Corp, punctuation) are merged.
10510(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 5, 2016 | K152930 | PeriFlux6000 Perimed AB, SE | DPW |
| Oct 22, 2013 | K131253 | PERIFLUX 6000 Perimed AB, SE | LKD |
| Jul 3, 2012 | K120884 | PERICAM PSI Perimed AB, SE | DPT |
| Nov 6, 2001 | K011899 | PF 5050 PRESSURE UNIT, MODEL PF 5050 Perimed AB, SE | DPW |
| Sep 23, 1999 | K990960 | PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040) Perimed, Inc. | LKD |
| May 28, 1998 | K974285 | PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT Perimed, Inc. | DPW |
| Apr 18, 1994 | K935495 | PF404/409/410/411/416/418 W/PF319:0/319:1/319:2 Perimed, Inc. | GEX |
| Dec 7, 1993 | K932068 | PERITEMP PF 4005 HEATER Perimed, Inc. | DPW |
| Feb 3, 1993 | K922368 | PERIFLUX PF4001 LASER DOPPLER FLOWMETER Perimed, Inc. | DPW |
| Jun 20, 1989 | K890828 | PERIFLUX PF3 Perimed, Inc. | DPW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||