510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023955Substantially Equivalent

Bd Viper Instrument

Becton Dickinson & Co, Sparks MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023955 is the FDA 510(k) clearance record for BD VIPER INSTRUMENT, a class I device, cleared for Becton, Dickinson & CO on under FDA product code JQW (Station, Pipetting And Diluting, For Clinical Use). FDA records list 345 510(k) clearances for Becton, Dickinson & CO, from to . As of , FDA records show no recalls naming K023955.

Clearance record

Decision date
Received
(209 days to decision)
Product code
JQW Station, Pipetting And Diluting, For Clinical Use
Regulation
21 CFR 862.2750
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Becton, Dickinson & CO 7loveton Cir., Sparks MD
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JQW

Trailing 12 months

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

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