GIO — Tube, Collection, Capillary Blood Class I

FDA Device Classification

Classification Details

Product Code
GIO
Device Class
Class I
Regulation Number
864.6150
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K972969innovative medical technologiesQUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMSeptember 22, 1997
K941291sherwood medicalMONOJECT SAMPLETTE SEPARATOR TUBEOctober 27, 1994
K894851humagenTRU-TRAXSeptember 29, 1989
K885324medical products searchHEMA(PRO)TEC(TION)February 17, 1989
K885138coeur laboratoriesCAPILLARY TUBE, BLOOD COLLECTIONFebruary 7, 1989
K884623safe-tec clinical productsSAFE-TEC CAPILLARY BLOOD COLLECTION TUBEDecember 1, 1988
K881187helps productsNATELSON TUBES, HEPARIN AND PLAINMay 6, 1988
K881262helps productsCARAWAY TUBES, HEPARIN AND PLAINMay 6, 1988
K875061sherwood medicalMONOJECT SAMPLETTE AMBER CAPILLARY SERUM SEPARATORJanuary 12, 1988
K873647ventrex laboratoriesVENTRESCREEN CAPILLARY BLOOD COLLECTION TUBEOctober 20, 1987
K850806corning medical and scientificCORNING BLOOD COLLECTION CAPILLARY TUBESMarch 25, 1985
K843608medical technomicsCAPILLARY BLOOD COLLECTION TUBENovember 30, 1984
K843892abco dealersMICRO HEMATOCRIT CAPILLARY TUBESNovember 13, 1984
K843361medical technomicsMINICAPSSeptember 21, 1984
K843362medical technomicsRINGCAPSSeptember 21, 1984
K832578sherwood medicalMONOJET SAMPLETTE ADAPTERSAugust 31, 1983
K812922american dadeS/P SURE-CAP CNovember 6, 1981
K812923american dadeS/P SURE-CAP NNovember 6, 1981
K812970american dadeS/P CAPILLARY TUBES, HEPARINIZED (3A)November 6, 1981
K812921american dadeS/P SURE-CAPNovember 6, 1981