510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K002885Substantially Equivalent

Dade Pfa-100 Platelet Function Analyzer Model-100, Dade Pfa Collegen/epinephrine Test Cartride, Dade Pfa Colleagen /Adp

Siemens Healthcare Diagnostics Inc., P.O. Box 6101, Newark DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002885 is the FDA 510(k) clearance record for DADE PFA-100 PLATELET FUNCTION ANALYZER MODEL-100, DADE PFA COLLEGEN/EPINEPHRINE TEST CARTRIDE, DADE PFA COLLEAGEN /ADP, a class II device, cleared for Dade Behring, Inc. on under FDA product code JOZ (System, Automated Platelet Aggregation). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K002885.

Clearance record

Decision date
Received
(279 days to decision)
Product code
JOZ System, Automated Platelet Aggregation
Regulation
21 CFR 864.5700
Device class
Class II
Review panel
Hematology
Applicant
Dade Behring, Inc. Glasgow Business Community;, P.O. Box 6101, Newark DE
510(k) summary
Summary
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JOZ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260