510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062114Substantially Equivalent

Ceruloplasmin, Model 2055953

Roche Diagnostics GmbH, Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062114 is the FDA 510(k) clearance record for CERULOPLASMIN, MODEL 2055953, a class II device, cleared for Roche Diagnostics Corp. on under FDA product code CHN (Immunochemical, Ceruloplasmin). FDA records list 465 510(k) clearances for Roche Diagnostics Corp., from to . As of , FDA records show no recalls naming K062114.

Clearance record

Decision date
Received
(191 days to decision)
Product code
CHN Immunochemical, Ceruloplasmin
Regulation
21 CFR 866.5210
Device class
Class II
Review panel
Immunology
Applicant
Roche Diagnostics Corp. 9115 Hague Rd., Indianapolis IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CHN

Trailing 12 months

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

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