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FDA 510(k)

CSI LIQUID OXYGEN SYSTEM

K-Number: K863556 · 1986-10-15

Decision Date1986-10-15
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CSI LIQUID OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cryogenic Services, Inc.. It received FDA 510(k) clearance on 1986-10-15 under 510(k) number K863556. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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