510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K971981Substantially Equivalent

Ls Series 200 Flovision System

Systam, Elfers FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K971981 is the FDA 510(k) clearance record for LS SERIES 200 FLOVISION SYSTEM, a class II device, cleared for Systam on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list one 510(k) clearance for Systam. As of , FDA records show no recalls naming K971981.

Clearance record

Decision date
Received
(572 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Systam P.O. Box 1108, Elfers FL
510(k) summary
Summary
Third party review
No

Clearances, product code CAF

Trailing 12 months
4 clearances under product code CAF in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAF, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260