9100 MUTIGAS MONITOR
K-Number: K941971 · 1994-11-21
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Device Summary
Frequently Asked Questions
What is the 9100 MUTIGAS MONITOR?
9100 MUTIGAS MONITOR is a medical device that received FDA 510(k) clearance on 1994-11-21. The listed applicant is Bci Intl., Inc.. The 510(k) number is K941971.
When did 9100 MUTIGAS MONITOR receive FDA 510(k) clearance?
9100 MUTIGAS MONITOR received FDA 510(k) clearance on 1994-11-21, under 510(k) number K941971.
Who is the listed applicant for 9100 MUTIGAS MONITOR?
The FDA 510(k) record lists Bci Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 9100 MUTIGAS MONITOR?
The FDA product code for 9100 MUTIGAS MONITOR is CCK.
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 Bci Intl., 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: CCK)
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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