RHINOTHERM ULTRA 2— 510(k) K894734

Substantially Equivalent

Twinmed Products, Inc.

FDA 510(k) clearance K894734 for RHINOTHERM ULTRA 2, Substantially Equivalent on 1990-02-16. Applicant: Twinmed Products, Inc.. Device class: 1.

Clearance details

Applicant: Twinmed Products, Inc.
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1989-07-24
Decision date: 1990-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

Download summary PDF View on FDA.gov ↗

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