510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K993558Substantially Equivalent

Ezflow Max, Model 1007

Piper Medical Products, West Sacramento CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993558 is the FDA 510(k) clearance record for EZFLOW MAX, MODEL 1007, a class II device, cleared for Piper Medical Products on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 3 510(k) clearances for Piper Medical Products, from to . As of , FDA records show no recalls naming K993558.

Clearance record

Decision date
Received
(23 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Piper Medical Products 4007 Seaport Blvd., West Sacramento CA
510(k) summary
Statement
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