510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950393Substantially Equivalent

Ace(tm) Cedia(r) Ferritin Assay

Schiapparelli Biosystems, Inc., Columbia MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950393 is the FDA 510(k) clearance record for ACE(TM) CEDIA(R) FERRITIN ASSAY, a class II device, cleared for Schiapparelli Biosystems, Inc. on under FDA product code JMG (Radioimmunoassay (Two-Site Solid Phase), Ferritin). FDA records list 24 510(k) clearances for Schiapparelli Biosystems, Inc., from to . As of , FDA records show no recalls naming K950393.

Clearance record

Decision date
Received
(104 days to decision)
Product code
JMG Radioimmunoassay (Two-Site Solid Phase), Ferritin
Regulation
21 CFR 866.5340
Device class
Class II
Review panel
Immunology
Applicant
Schiapparelli Biosystems, Inc. 9033 Red Branch Rd., Columbia MD
510(k) summary
Summary
Third party review
No

Clearances, product code JMG

Trailing 12 months

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

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