510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955906Substantially Equivalent

Boehringer Mannheim Igg Assay

Boehringer Mannheim Corp., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955906 is the FDA 510(k) clearance record for BOEHRINGER MANNHEIM IGG ASSAY, a class II device, cleared for Boehringer Mannheim Corp. on under FDA product code DFZ (Igg (Gamma Chain Specific), Antigen, Antiserum, Control). FDA records list 340 510(k) clearances for Boehringer Mannheim Corp., from to . As of , FDA records show no recalls naming K955906.

Clearance record

Decision date
Received
(42 days to decision)
Product code
DFZ Igg (Gamma Chain Specific), Antigen, Antiserum, Control
Regulation
21 CFR 866.5510
Device class
Class II
Review panel
Immunology
Applicant
Boehringer Mannheim Corp. 9115 Hague Rd., P.O. Box 50457, Indianapolis IN
510(k) summary
Summary
Third party review
No

Clearances, product code DFZ

Trailing 12 months

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

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