Exelint Intl. Co.
Culver City, CA, US
Exelint Intl. Co. appears in FDA device records in Culver City, CA. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Exelint Intl. Co. between 2000 and 2010. The busiest year on record is 2002, with 4. The most recent is 2010, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 1 |
| 2001 | 3 |
| 2002 | 4 |
| 2003 | 2 |
| 2005 | 1 |
| 2010 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K092172 | EXEL I.V. EXTENSION SET | FPA | Substantially Equivalent | |
| K052103 | EXEL SECURE TOUCH II SAFETY SYRINGE | MEG | Substantially Equivalent | |
| K031500 | EXCEL PRIMARY SOLUTION SET | FPA | Substantially Equivalent | |
| K011754 | EXEL SECURETOUCH PTP SYRINGE | MEG | Substantially Equivalent | |
| K020533 | EXEL VACULET BLOOD COLLECTION SET | FPA | Substantially Equivalent | |
| K022406 | EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET | FMI | Substantially Equivalent | |
| K011757 | EXEL COMFORTPOINT INSULIN PEN NEEDLE | FMI | Substantially Equivalent | |
| K012879 | EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE | FPA | Substantially Equivalent | |
| K013037 | EXCEL A.V FISUTAL NEEDLE SET | FIE | Substantially Equivalent | |
| K011405 | EXEL INJECTION PLUG WITH CAP | FPA | Substantially Equivalent | |
| K010404 | EXEL I.V. ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K992039 | EXEL I.V. BLOOD LINE SET | FJK | 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain