Exel Intl.
Culver City, CA, US
Exel Intl. appears in FDA device records in Culver City, CA. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Exel Intl. between 1986 and 2000. The busiest year on record is 1986, with 7. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 7 |
| 1990 | 7 |
| 1993 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K992290 | EXEL INJECTION PLUG WITH CAP | FPA | Substantially Equivalent | |
| K963658 | EXEL AVF SINGLE NEEDLE | FMI | Substantially Equivalent | |
| K963659 | EXEL I.V. ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K926119 | EXEL HUBER INFUSION SET ROTATING WING | FPA | Substantially Equivalent | |
| K904685 | EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y) | FPA | Substantially Equivalent | |
| K903945 | EXEL A-V FISTULA SET | FIE | Substantially Equivalent | |
| K895770 | EXEL HUBER INFUSION SET | FPA | Substantially Equivalent | |
| K895772 | EXEL INDWELLING CATHETER | FDZ | Substantially Equivalent | |
| K895771 | EXEL SPINAL NEEDLES | FMI | Substantially Equivalent | |
| K895769 | EXEL HUBER NEEDLE | FMI | Substantially Equivalent | |
| K895768 | EXEL SAFELET CATHETER | FOZ | Substantially Equivalent | |
| K862492 | EXEL THREE-WAY STOPCOCK | FMG | Substantially Equivalent | |
| K861449 | VACUUM BLOOD COLLECTING SYSTEM (NEO-TUBE) | GIM | Substantially Equivalent | |
| K862491 | EXEL BUTTERFLY SCALP VEIN SET | FPA | Substantially Equivalent | |
| K861152 | EXEL VACUUM BLOOD COLLECTING SYSTEM | FMI | Substantially Equivalent | |
| K861153 | DISPOSABLE SYRINGES AND HYPODERMIC NEEDLES | FMF | Substantially Equivalent | |
| K861151 | SUEL BLOOD LANCET | FMK | Substantially Equivalent | |
| K861150 | EXEL DENTAL NEEDLE | DZM | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- FDZAttachment, Eyepiece, For Insertion Of Prescription Lens
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- DZMNeedle, Dental
- FIENeedle, Fistula
- FMINeedle, Hypodermic, Single Lumen
- FPASet, Administration, Intravascular
- FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- FMGStopcock, I.V. Set
- FMFSyringe, Piston
- GIMTubes, Vacuum Sample, With Anticoagulant
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