CSI LIQUID OXYGEN SYSTEM
K-Number: K863556 · 1986-10-15
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Device Summary
Frequently Asked Questions
What is the CSI LIQUID OXYGEN SYSTEM?
CSI LIQUID OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 1986-10-15. The listed applicant is Cryogenic Services, Inc.. The 510(k) number is K863556.
When did CSI LIQUID OXYGEN SYSTEM receive FDA 510(k) clearance?
CSI LIQUID OXYGEN SYSTEM received FDA 510(k) clearance on 1986-10-15, under 510(k) number K863556.
Who is the listed applicant for CSI LIQUID OXYGEN SYSTEM?
The FDA 510(k) record lists Cryogenic Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CSI LIQUID OXYGEN SYSTEM?
The FDA product code for CSI LIQUID OXYGEN SYSTEM 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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