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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
510(k) clearance decisions for Greiner America, Inc., by decision year
YearClearances
19963
19974
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K971220GREINER VACUETTE BLOOD COLLECTION TUBEJKASubstantially Equivalent
K971239GREINER VACUETTE BLOOD COLLECTION TUBEJKASubstantially Equivalent
K971236GREINER VACUETTE BLOOD COLLECTION TUBEJKASubstantially Equivalent
K971221GREINER VACUETTE BLOOD COLLECTION TUBEGIMSubstantially Equivalent
K960860GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3JKASubstantially Equivalent
K960858GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATORJKASubstantially Equivalent
K960857GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATORJKASubstantially 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