510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K962161Substantially Equivalent

Baxter Nebulizer Cap Model 2D0868

Baxter Healthcare Corporation, Tarpon Springs FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962161 is the FDA 510(k) clearance record for BAXTER NEBULIZER CAP MODEL 2D0868, a class II device, cleared for Baxter Healthcare Corp on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K962161.

Clearance record

Decision date
Received
(72 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Baxter Healthcare Corp 40178 u.s. 19 N., Tarpon Springs FL
510(k) summary
Summary
Third party review
No

Clearances, product code CAF

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