510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993907Substantially Equivalent

Viridia Information Center Software for M3154a Opt C22

Agilent Technologies, Inc., Andover MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K993907 is the FDA 510(k) clearance record for VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22, a class II device, cleared for Agilent Technologies, Inc. on under FDA product code MHD (Pump, Infusion, Gallstone Dissolution). FDA records list 51 510(k) clearances for Agilent Technologies, Inc., from to . As of , FDA records show no recalls naming K993907.

Clearance record

Decision date
Received
(19 days to decision)
Product code
MHD Pump, Infusion, Gallstone Dissolution
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Agilent Technologies, Inc. 3000 Minuteman Rd., Andover MA
510(k) summary
Summary
Third party review
No

Clearances, product code MHD

Trailing 12 months

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

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