QA PRESSURE MEASUREMENT SYSTEM
K-Number: K925052 · 1993-03-09
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Device Summary
Frequently Asked Questions
What is the QA PRESSURE MEASUREMENT SYSTEM?
QA PRESSURE MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-09. The listed applicant is Gabel Medical Instruments, Ltd.. The 510(k) number is K925052.
When did QA PRESSURE MEASUREMENT SYSTEM receive FDA 510(k) clearance?
QA PRESSURE MEASUREMENT SYSTEM received FDA 510(k) clearance on 1993-03-09, under 510(k) number K925052.
Who is the listed applicant for QA PRESSURE MEASUREMENT SYSTEM?
The FDA 510(k) record lists Gabel Medical Instruments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QA PRESSURE MEASUREMENT SYSTEM?
The FDA product code for QA PRESSURE MEASUREMENT SYSTEM is JFC.
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: JFC)
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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