RESPIRIZER— 510(k) K810335

Name: FDA 510(k) clearance K810335
Creator: U.S. Food and Drug Administration
Published: 1981-03-20

Substantially Equivalent

Respirizer Co., Div. Campillary Systems, Inc.

FDA 510(k) clearance K810335 for RESPIRIZER, Substantially Equivalent on 1981-03-20. Applicant: Respirizer Co., Div. Campillary Systems, Inc.. Device class: 1.

Clearance details

Applicant: Respirizer Co., Div. Campillary Systems, Inc.
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1981-02-09
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KFZ

view all

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

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