510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K133951Substantially Equivalent

Smarttouch

Nexus6, Ltd., Auckland, NZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133951 is the FDA 510(k) clearance record for SMARTTOUCH, a class II device, cleared for Nexus6, Ltd. on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 2 510(k) clearances for Nexus6, Ltd., from to . As of , FDA records show no recalls naming K133951.

Clearance record

Decision date
Received
(123 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Nexus6, Ltd. 8 Commerce St., Auckland, NZ
510(k) summary
Summary PDF
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