510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K900856Substantially Equivalent

Ven-O-Vac Blood Collection Vacuum Tubes

Artefactos de Vidrio S.A. de C.V., Mexico, MX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900856 is the FDA 510(k) clearance record for VEN-O-VAC BLOOD COLLECTION VACUUM TUBES, a class II device, cleared for Artefactos DE Vidrio S.A. DE C.V. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list one 510(k) clearance for Artefactos DE Vidrio S.A. DE C.V. As of , FDA records show no recalls naming K900856.

Clearance record

Decision date
Received
(210 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Artefactos DE Vidrio S.A. DE C.V. Canela # 346, Mexico, MX
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260