510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K951965Substantially Equivalent

Dako Labeled Streptavidin-Biotin 2 Kit, and Envision

Dako Corp., Carpinteria CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951965 is the FDA 510(k) clearance record for DAKO LABELED STREPTAVIDIN-BIOTIN 2 KIT, AND ENVISION, a class II device, cleared for Dako Corp. on under FDA product code DEH (Lambda, Antigen, Antiserum, Control). FDA records list 25 510(k) clearances for Dako Corp., from to . As of , FDA records show no recalls naming K951965.

Clearance record

Decision date
Received
(435 days to decision)
Product code
DEH Lambda, Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
Device class
Class II
Review panel
Immunology
Applicant
Dako Corp. 6392 Via Real, Carpinteria CA
510(k) summary
Summary
Third party review
No

Clearances, product code DEH

Trailing 12 months

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

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