DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF
K-Number: K896788 · 1990-01-19
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Device Summary
Frequently Asked Questions
What is the DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF?
DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Advanced Medical Instruments, Inc.. The 510(k) number is K896788.
When did DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF receive FDA 510(k) clearance?
DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF received FDA 510(k) clearance on 1990-01-19, under 510(k) number K896788.
Who is the listed applicant for DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF?
The FDA 510(k) record lists Advanced Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF?
The FDA product code for DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF is DXQ.
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 Advanced Medical Instruments, 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: DXQ)
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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