510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914685Substantially Equivalent

866.5750 Radioallergosorbent Immunlogical Test Sys

In Vitro Technologies, Inc., Arlington TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914685 is the FDA 510(k) clearance record for 866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYS, a class II device, cleared for In Vitro Technologies, Inc. on under FDA product code DHB (System, Test, Radioallergosorbent (Rast) Immunological). FDA records list 7 510(k) clearances for In Vitro Technologies, Inc., from to . As of , FDA records show no recalls naming K914685.

Clearance record

Decision date
Received
(332 days to decision)
Product code
DHB System, Test, Radioallergosorbent (Rast) Immunological
Regulation
21 CFR 866.5750
Device class
Class II
Review panel
Immunology
Applicant
In Vitro Technologies, Inc. 2100 Rd. To Six Flags, E., Arlington TX
510(k) summary
Statement
Third party review
No

Clearances, product code DHB

Trailing 12 months
7 clearances under product code DHB in the twelve months to October 2026, July 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DHB, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20261
June 20261
July 20262
August 20260
September 20261
October 20260