510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811713Substantially Equivalent

Avi-D Control

Ortho Diagnostic Systems, Inc., Carpinteria CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811713 is the FDA 510(k) clearance record for AVI-D CONTROL, a class II device, cleared for Ortho Diagnostic Systems, Inc. on under FDA product code KSF (Kit, Quality Control For Blood Banking Reagents). FDA records list 126 510(k) clearances for Ortho Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K811713.

Clearance record

Decision date
Received
(128 days to decision)
Product code
KSF Kit, Quality Control For Blood Banking Reagents
Regulation
21 CFR 864.9650
Device class
Class II
Review panel
Hematology
Applicant
Ortho Diagnostic Systems, Inc. 125 Mark Ave., Carpinteria CA
Third party review
No

Clearances, product code KSF

Trailing 12 months

FDA records hold no clearances under product code KSF in the trailing twelve months.

FDA records show no clearances under product code KSF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KSF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260