PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT
K-Number: K963956 · 1996-12-09
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Device Summary
Frequently Asked Questions
What is the PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT?
PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT is a medical device that received FDA 510(k) clearance on 1996-12-09. The listed applicant is Southern Research, Inc.. The 510(k) number is K963956.
When did PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT receive FDA 510(k) clearance?
PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT received FDA 510(k) clearance on 1996-12-09, under 510(k) number K963956.
Who is the listed applicant for PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT?
The FDA 510(k) record lists Southern Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT?
The FDA product code for PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT is BYJ.
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: BYJ)
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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