CM7000 REMOTE INDICATOR
K-Number: K931287 · 1993-07-01
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Device Summary
Frequently Asked Questions
What is the CM7000 REMOTE INDICATOR?
CM7000 REMOTE INDICATOR is a medical device that received FDA 510(k) clearance on 1993-07-01. The listed applicant is Canadian Monaghan , Ltd.. The 510(k) number is K931287.
When did CM7000 REMOTE INDICATOR receive FDA 510(k) clearance?
CM7000 REMOTE INDICATOR received FDA 510(k) clearance on 1993-07-01, under 510(k) number K931287.
Who is the listed applicant for CM7000 REMOTE INDICATOR?
The FDA 510(k) record lists Canadian Monaghan , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CM7000 REMOTE INDICATOR?
The FDA product code for CM7000 REMOTE INDICATOR is CAP.
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 Canadian Monaghan , Ltd. 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: CAP)
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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