CPAP/PRO CPAP INTERFACE
K-Number: K992384 · 1999-12-01
Advertisement
Device Summary
Frequently Asked Questions
What is the CPAP/PRO CPAP INTERFACE?
CPAP/PRO CPAP INTERFACE is a medical device that received FDA 510(k) clearance on 1999-12-01. The listed applicant is Stevenson Industries, Inc.. The 510(k) number is K992384.
When did CPAP/PRO CPAP INTERFACE receive FDA 510(k) clearance?
CPAP/PRO CPAP INTERFACE received FDA 510(k) clearance on 1999-12-01, under 510(k) number K992384.
Who is the listed applicant for CPAP/PRO CPAP INTERFACE?
The FDA 510(k) record lists Stevenson Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CPAP/PRO CPAP INTERFACE?
The FDA product code for CPAP/PRO CPAP INTERFACE is BZD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BZD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement