FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE

K Number: K873647 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
21
Applicant Total
82
Review Days
41

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Basic Information

Device Name
VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE
K Number
K873647
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.6150
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Ventrex Laboratories, Inc.
Date Received
September 9, 1987
Decision Date
October 20, 1987
Product Code
GIO
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GIO Tube, Collection, Capillary Blood

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Other Clearances by Ventrex Laboratories, Inc.

K Number Device Name
K914554 SPECIFIC IGE EIA-TURBO ASSAY
K913833 VENTREX ALLERGEN DISC
K913434 VENTREX COATED TUBE INTACT PTH
K905612 VENTREX COATED TUBE IGE RADIOIMMUNOASSAY
K905636 VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
K905247 SHBG IRMA KIT
K904330 TURBO-RAST SPECIFIC IGE ASSAY
K903000 TURBO-RAST SPECIFIC IGE ASSAY
K897083 VENTRESIGN STREP A TEST
K895648 COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.
Search all 82 clearances from Ventrex Laboratories, Inc. →