Greiner America, Inc.
Wilmington, DE, US
Greiner America, Inc. appears in FDA device records in Wilmington, DE. 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 Greiner America, Inc. between 1996 and 1997. The busiest year on record is 1997, with 4. The most recent is 1997, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1996 | 3 |
| 1997 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K971220 | GREINER VACUETTE BLOOD COLLECTION TUBE | JKA | Substantially Equivalent | |
| K971239 | GREINER VACUETTE BLOOD COLLECTION TUBE | JKA | Substantially Equivalent | |
| K971236 | GREINER VACUETTE BLOOD COLLECTION TUBE | JKA | Substantially Equivalent | |
| K971221 | GREINER VACUETTE BLOOD COLLECTION TUBE | GIM | Substantially Equivalent | |
| K960860 | GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 | JKA | Substantially Equivalent | |
| K960858 | GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR | JKA | Substantially Equivalent | |
| K960857 | GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR | JKA | 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
