VENOUS PRESSURE MONITOR, MF 35 LF
K-Number: K790668 · 1979-05-23
Advertisement
Device Summary
Frequently Asked Questions
What is the VENOUS PRESSURE MONITOR, MF 35 LF?
VENOUS PRESSURE MONITOR, MF 35 LF is a medical device that received FDA 510(k) clearance on 1979-05-23. The listed applicant is Deco Medical, Inc.. The 510(k) number is K790668.
When did VENOUS PRESSURE MONITOR, MF 35 LF receive FDA 510(k) clearance?
VENOUS PRESSURE MONITOR, MF 35 LF received FDA 510(k) clearance on 1979-05-23, under 510(k) number K790668.
Who is the listed applicant for VENOUS PRESSURE MONITOR, MF 35 LF?
The FDA 510(k) record lists Deco Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENOUS PRESSURE MONITOR, MF 35 LF?
The FDA product code for VENOUS PRESSURE MONITOR, MF 35 LF is KRK.
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: KRK)
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.
Advertisement