PROXIMA 1 PH MONITOR
K-Number: K881706 · 1988-07-12
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Device Summary
Frequently Asked Questions
What is the PROXIMA 1 PH MONITOR?
PROXIMA 1 PH MONITOR is a medical device that received FDA 510(k) clearance on 1988-07-12. The listed applicant is Technomanagement, Inc. C/O C.G.. The 510(k) number is K881706.
When did PROXIMA 1 PH MONITOR receive FDA 510(k) clearance?
PROXIMA 1 PH MONITOR received FDA 510(k) clearance on 1988-07-12, under 510(k) number K881706.
Who is the listed applicant for PROXIMA 1 PH MONITOR?
The FDA 510(k) record lists Technomanagement, Inc. C/O C.G. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROXIMA 1 PH MONITOR?
The FDA product code for PROXIMA 1 PH MONITOR is FFT.
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.
Related Devices (Code: FFT)
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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