510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K980089Substantially Equivalent

3600 Presure Infusor, Sigmacon 3600, Lapro Flow 3000

Valley West, Inc., Meridian TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980089 is the FDA 510(k) clearance record for 3600 PRESURE INFUSOR, SIGMACON 3600, LAPRO FLOW 3000, a class II device, cleared for Valley West, Inc. on under FDA product code FRN (Pump, Infusion). FDA records list 3 510(k) clearances for Valley West, Inc., from to . As of , FDA records show no recalls naming K980089.

Clearance record

Decision date
Received
(74 days to decision)
Product code
FRN Pump, Infusion
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Valley West, Inc. Hwy. 6 N., P.O. Box 678, Meridian TX
510(k) summary
Summary
Third party review
No

Clearances, product code FRN

Trailing 12 months
2 clearances under product code FRN in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FRN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260