ANAEROBIC CARBON DIOXIDE
K-Number: K822752 · 1982-10-22
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Device Summary
Frequently Asked Questions
What is the ANAEROBIC CARBON DIOXIDE?
ANAEROBIC CARBON DIOXIDE is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Liquid Carbonic Corp.. The 510(k) number is K822752.
When did ANAEROBIC CARBON DIOXIDE receive FDA 510(k) clearance?
ANAEROBIC CARBON DIOXIDE received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822752.
Who is the listed applicant for ANAEROBIC CARBON DIOXIDE?
The FDA 510(k) record lists Liquid Carbonic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANAEROBIC CARBON DIOXIDE?
The FDA product code for ANAEROBIC CARBON DIOXIDE 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 Liquid Carbonic Corp. 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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