ALPINE PORTABLE OXYGEN GENERATOR
K-Number: K881802 · 1988-07-08
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Device Summary
Frequently Asked Questions
What is the ALPINE PORTABLE OXYGEN GENERATOR?
ALPINE PORTABLE OXYGEN GENERATOR is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Mountain Medical Equipment, Inc.. The 510(k) number is K881802.
When did ALPINE PORTABLE OXYGEN GENERATOR receive FDA 510(k) clearance?
ALPINE PORTABLE OXYGEN GENERATOR received FDA 510(k) clearance on 1988-07-08, under 510(k) number K881802.
Who is the listed applicant for ALPINE PORTABLE OXYGEN GENERATOR?
The FDA 510(k) record lists Mountain Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALPINE PORTABLE OXYGEN GENERATOR?
The FDA product code for ALPINE PORTABLE OXYGEN GENERATOR is CAW.
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 Mountain Medical Equipment, 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: CAW)
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.
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