ALADDIN MONITORING OXYGEN/AIR MIXER
K-Number: K960359 · 1996-04-24
Advertisement
Device Summary
Frequently Asked Questions
What is the ALADDIN MONITORING OXYGEN/AIR MIXER?
ALADDIN MONITORING OXYGEN/AIR MIXER is a medical device that received FDA 510(k) clearance on 1996-04-24. The listed applicant is Hamilton Medical, Inc.. The 510(k) number is K960359.
When did ALADDIN MONITORING OXYGEN/AIR MIXER receive FDA 510(k) clearance?
ALADDIN MONITORING OXYGEN/AIR MIXER received FDA 510(k) clearance on 1996-04-24, under 510(k) number K960359.
Who is the listed applicant for ALADDIN MONITORING OXYGEN/AIR MIXER?
The FDA 510(k) record lists Hamilton Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALADDIN MONITORING OXYGEN/AIR MIXER?
The FDA product code for ALADDIN MONITORING OXYGEN/AIR MIXER is BZR.
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.
Other records listing Hamilton Medical, Inc. as applicant
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: BZR)
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