CARBON DIOXIDE - DST
K-Number: K952410 · 1995-10-05
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Device Summary
Frequently Asked Questions
What is the CARBON DIOXIDE - DST?
CARBON DIOXIDE - DST is a medical device that received FDA 510(k) clearance on 1995-10-05. The listed applicant is Trace America, Inc.. The 510(k) number is K952410.
When did CARBON DIOXIDE - DST receive FDA 510(k) clearance?
CARBON DIOXIDE - DST received FDA 510(k) clearance on 1995-10-05, under 510(k) number K952410.
Who is the listed applicant for CARBON DIOXIDE - DST?
The FDA 510(k) record lists Trace America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARBON DIOXIDE - DST?
The FDA product code for CARBON DIOXIDE - DST is KHS.
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 Trace America, 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: KHS)
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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