CALIBRATION GAS
K-Number: K932520 · 1993-08-19
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Device Summary
Frequently Asked Questions
What is the CALIBRATION GAS?
CALIBRATION GAS is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is Cryodyne Technologies, Inc.. The 510(k) number is K932520.
When did CALIBRATION GAS receive FDA 510(k) clearance?
CALIBRATION GAS received FDA 510(k) clearance on 1993-08-19, under 510(k) number K932520.
Who is the listed applicant for CALIBRATION GAS?
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 CALIBRATION GAS?
The FDA product code for CALIBRATION GAS is BXK.
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: BXK)
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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