510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895688Substantially Equivalent

Nobles-Lai Engineering Infusion Pump

Nobles-Lai Engineering, Inc., Santa Ana CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895688 is the FDA 510(k) clearance record for NOBLES-LAI ENGINEERING INFUSION PUMP, a class II device, cleared for Nobles-Lai Engineering, Inc. on under FDA product code DQI (Withdrawal/Infusion Pump). FDA records list 5 510(k) clearances for Nobles-Lai Engineering, Inc., from to . As of , FDA records show no recalls naming K895688.

Clearance record

Decision date
Received
(157 days to decision)
Product code
DQI Withdrawal/Infusion Pump
Regulation
21 CFR 870.1800
Device class
Class II
Review panel
Cardiovascular
Applicant
Nobles-Lai Engineering, Inc. 3033 S. Harbor Blvd., Santa Ana CA
Third party review
No

Clearances, product code DQI

Trailing 12 months

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

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