Imed Corp.
San Diego, CA, US
Imed Corp. appears in FDA device records in San Diego, CA. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Imed Corp. between 1985 and 1996. The busiest year on record is 1995, with 5. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 3 |
| 1986 | 1 |
| 1987 | 4 |
| 1988 | 2 |
| 1989 | 1 |
| 1990 | 1 |
| 1992 | 2 |
| 1993 | 2 |
| 1994 | 1 |
| 1995 | 5 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960512 | GEMINI PC-ITX | FRN | Substantially Equivalent | |
| K953896 | THE IMED AMBULATORY INFUSION PUMP, ADMINISTRATION SETS | FRN | Substantially Equivalent | |
| K950153 | VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO SAFSITE(TM) VALVES | FPA | Substantially Equivalent | |
| K951922 | ADMINISTRATION SETS WITH BALL FLOAT | FPA | Substantially Equivalent | |
| K950419 | THE IMED ORION INFUSION PUMP AND ADMINISTRATION SETS | FRN | Substantially Equivalent | |
| K944320 | VENTED/NON-VENTED GEMINI ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K945070 | VERSASAE PLASTIC CANNULA- 11 GAUGE | FPA | Substantially Equivalent | |
| K931173 | PRIMARY ADMIN SET W/UNIV SP-MAN BELOW/ABV PUMP CH | FPA | Substantially Equivalent | |
| K933144 | GEMINI VOLUMETRIC INFUSION PUMP/CONTROLLER | FRN | Substantially Equivalent | |
| K924718 | SHROUDED NEEDLE DEVICES | FPA | Substantially Equivalent | |
| K921378 | IMED MODEL PC-4 VOLUMETRIC INFUSION PUMP/CONTROLLE | FRN | Substantially Equivalent | |
| K913658 | IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD | MEB | Substantially Equivalent | |
| K895797 | IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE | FRN | Substantially Equivalent | |
| K894842 | IMED GEMINI 12 NONVENTED Y-TYPE BLOOD/SOLUTION ADM | FPA | Substantially Equivalent | |
| K883993 | MODIFIED IMED GEMINI PC-1 INFUSION PUMP | FRN | Substantially Equivalent | |
| K880479 | IMED(R) GEMINI(TM) PC-1 VOLUMETRIC INFUSION PUMP | FRN | Substantially Equivalent | |
| K872952 | ULTRASONIC AIR-IN-LINE DETECTOR (AILD) | FRN | Substantially Equivalent | |
| K870656 | IMED(R) 980C VOLUMETRIC INFUSION PUMP | FRN | Substantially Equivalent | |
| K870992 | IMED(R) MODEL 965A VOLUMETRIC INFUSION PUMP | FRN | Substantially Equivalent | |
| K870991 | IMED(R) MODEL 960A VOLUMETRIC INFUSION PUMP | FRN | Substantially Equivalent | |
| K862295 | MODEL PC-2 VOLUMETRIC INFUSION PUMP/CONTROLLER | FRN | Substantially Equivalent | |
| K851360 | IMED GRAVISET INTRAVASCULAR ADMIN. SET | FRN | Substantially Equivalent | |
| K850653 | IMED 440 INFUSION PUMP & ADMINISTRATION SET | FRN | Substantially Equivalent | |
| K844915 | IMED 980 VOLUMETRIC INFUSION PUMP | FRN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain