COMPLETE TRAY CENTRAL VENOUS PRESSURE
K-Number: K792171 · 1979-11-13
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Device Summary
Frequently Asked Questions
What is the COMPLETE TRAY CENTRAL VENOUS PRESSURE?
COMPLETE TRAY CENTRAL VENOUS PRESSURE is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Stanco Medical, Inc.. The 510(k) number is K792171.
When did COMPLETE TRAY CENTRAL VENOUS PRESSURE receive FDA 510(k) clearance?
COMPLETE TRAY CENTRAL VENOUS PRESSURE received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792171.
Who is the listed applicant for COMPLETE TRAY CENTRAL VENOUS PRESSURE?
The FDA 510(k) record lists Stanco Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPLETE TRAY CENTRAL VENOUS PRESSURE?
The FDA product code for COMPLETE TRAY CENTRAL VENOUS PRESSURE is DYB.
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 Stanco Medical, 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: DYB)
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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