CHURCHILL MEDICAL SYSTEMS STOPCOCK
K-Number: K012157 · 2001-09-11
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Device Summary
Frequently Asked Questions
What is the CHURCHILL MEDICAL SYSTEMS STOPCOCK?
CHURCHILL MEDICAL SYSTEMS STOPCOCK is a medical device that received FDA 510(k) clearance on 2001-09-11. The listed applicant is Churchill Medical Systems, Inc.. The 510(k) number is K012157.
When did CHURCHILL MEDICAL SYSTEMS STOPCOCK receive FDA 510(k) clearance?
CHURCHILL MEDICAL SYSTEMS STOPCOCK received FDA 510(k) clearance on 2001-09-11, under 510(k) number K012157.
Who is the listed applicant for CHURCHILL MEDICAL SYSTEMS STOPCOCK?
The FDA 510(k) record lists Churchill Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHURCHILL MEDICAL SYSTEMS STOPCOCK?
The FDA product code for CHURCHILL MEDICAL SYSTEMS STOPCOCK is FMG.
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 Churchill Medical Systems, 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: FMG)
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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