510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833113Substantially Equivalent

Reporting Integrator 3392A

Hewlett-Packard Co., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833113 is the FDA 510(k) clearance record for REPORTING INTEGRATOR 3392A, a class I device, cleared for Hewlett-Packard Co. on under FDA product code LDM (Instrumentation, High Pressure Liquid Chromatography). FDA records list 246 510(k) clearances for Hewlett-Packard Co., from to . As of , FDA records show 2 recalls naming K833113.

Clearance record

Decision date
Received
(69 days to decision)
Product code
LDM Instrumentation, High Pressure Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Hewlett-Packard Co. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code LDM

Trailing 12 months

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

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