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FDA 510(k)

CTC 30, 40, 1 LIQUID OXYGEN LITERS

K-Number: K860738 · 1986-08-06

Decision Date1986-08-06
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CTC 30, 40, 1 LIQUID OXYGEN LITERS is the device name listed in this FDA 510(k) record. The listed applicant is Cryodyne Technologies, Inc.. It received FDA 510(k) clearance on 1986-08-06 under 510(k) number K860738. 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 CTC 30, 40, 1 LIQUID OXYGEN LITERS?

CTC 30, 40, 1 LIQUID OXYGEN LITERS is a medical device that received FDA 510(k) clearance on 1986-08-06. The listed applicant is Cryodyne Technologies, Inc.. The 510(k) number is K860738.

When did CTC 30, 40, 1 LIQUID OXYGEN LITERS receive FDA 510(k) clearance?

CTC 30, 40, 1 LIQUID OXYGEN LITERS received FDA 510(k) clearance on 1986-08-06, under 510(k) number K860738.

Who is the listed applicant for CTC 30, 40, 1 LIQUID OXYGEN LITERS?

The FDA 510(k) record lists Cryodyne Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTC 30, 40, 1 LIQUID OXYGEN LITERS?

The FDA product code for CTC 30, 40, 1 LIQUID OXYGEN LITERS 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.

Other records listing Cryodyne Technologies, 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: 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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