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510(k) K971220

GREINER VACUETTE BLOOD COLLECTION TUBE by Greiner America, Inc. — Product Code JKA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 4, 1997
Date Received
April 2, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
Device Class
Class II
Regulation Number
862.1675
Review Panel
CH
Submission Type

Other clearances by Greiner America, Inc.

  • K971236 — GREINER VACUETTE BLOOD COLLECTION TUBE (May 12, 1997)
  • K971239 — GREINER VACUETTE BLOOD COLLECTION TUBE (May 12, 1997)
  • K971221 — GREINER VACUETTE BLOOD COLLECTION TUBE (May 2, 1997)
  • K960860 — GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 (September 5, 1996)
  • K960858 — GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR (August 30, 1996)
  • K960857 — GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR (August 30, 1996)

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