PROCARE MONITOR B40
K-Number: K120598 · 2012-07-19
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Device Summary
Frequently Asked Questions
What is the PROCARE MONITOR B40?
PROCARE MONITOR B40 is a medical device that received FDA 510(k) clearance on 2012-07-19. The listed applicant is Ge Medical Systems China Co., Ltd.. The 510(k) number is K120598.
When did PROCARE MONITOR B40 receive FDA 510(k) clearance?
PROCARE MONITOR B40 received FDA 510(k) clearance on 2012-07-19, under 510(k) number K120598.
Who is the listed applicant for PROCARE MONITOR B40?
The FDA 510(k) record lists Ge Medical Systems China Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROCARE MONITOR B40?
The FDA product code for PROCARE MONITOR B40 is MHX.
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 Ge Medical Systems China Co., 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: MHX)
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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