INHALATION THERAPY NEBULIZER DEVICE— 510(k) K850711

Substantially Equivalent

Med USA

FDA 510(k) clearance K850711 for INHALATION THERAPY NEBULIZER DEVICE, Substantially Equivalent on 1985-06-05. Applicant: Med USA. Device class: 1.

Clearance details

Applicant: Med USA
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1985-02-22
Decision date: 1985-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KFZ

K950116 — THERASTEAM PERSONAL STEAM INHALER1995-02-10
K915603 — VIROTHERM HUMIDIFIER1992-10-22
K894734 — RHINOTHERM ULTRA 21990-02-16
K871661 — WH150 ROOM HUMIDIFIER1987-06-15
K871189 — SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 13801987-05-08

More clearances from Med USA

K896766 — TD-28 DISPOSABLE ELECTRODE1990-03-14
K862047 — COAGULATOR (8 CHANNEL)1986-09-29
K852492 — COAGULATOR1985-08-13
K841803 — A1 SYSTEME 8201/21985-02-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.