Erika, Inc.
Rockleigh, NJ, US
Erika, Inc. appears in FDA device records in Rockleigh, NJ. FDA records list 7 510(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
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Erika, Inc. in 1985.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K853134 | NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8 | FRN | Substantially Equivalent | |
| K852310 | NATURALYTE BICARBONATE CONCENTRATE-DRY PACK | FKQ | Substantially Equivalent | |
| K852309 | ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1 | FJK | Substantially Equivalent | |
| K850866 | TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L | KDI | Substantially Equivalent | |
| K850865 | TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1- | FJI | Substantially Equivalent | |
| K850655 | TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2 | FJI | Substantially Equivalent | |
| K850654 | TORAY INDUS. FILTRYZER HOLLOW FIBER ARTIFICIAL KID | FJI | 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