510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122162Substantially Equivalent

Aggreguide

Aggredyne, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122162 is the FDA 510(k) clearance record for AGGREGUIDE, a class II device, cleared for Aggredyne, Inc. on under FDA product code JOZ (System, Automated Platelet Aggregation). FDA records list 3 510(k) clearances for Aggredyne, Inc., from to . As of , FDA records show one recall naming K122162.

Clearance record

Decision date
Received
(518 days to decision)
Product code
JOZ System, Automated Platelet Aggregation
Regulation
21 CFR 864.5700
Device class
Class II
Review panel
Hematology
Applicant
Aggredyne, Inc. 11874 S. Evelyn Cir., Houston TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JOZ

Trailing 12 months

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

FDA records show no clearances under product code JOZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JOZ, 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