NEONATAL BLOOD PRESSURE CUFF
K-Number: K810838 · 1981-04-03
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Device Summary
Frequently Asked Questions
What is the NEONATAL BLOOD PRESSURE CUFF?
NEONATAL BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Invivo Research Labs, Inc.. The 510(k) number is K810838.
When did NEONATAL BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
NEONATAL BLOOD PRESSURE CUFF received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810838.
Who is the listed applicant for NEONATAL BLOOD PRESSURE CUFF?
The FDA 510(k) record lists Invivo Research Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEONATAL BLOOD PRESSURE CUFF?
The FDA product code for NEONATAL BLOOD PRESSURE 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 Invivo Research Labs, 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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