PRESSURE INFUSER
K-Number: K913751 · 1992-01-09
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Device Summary
Frequently Asked Questions
What is the PRESSURE INFUSER?
PRESSURE INFUSER is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Biomedical Dynamics, Inc.. The 510(k) number is K913751.
When did PRESSURE INFUSER receive FDA 510(k) clearance?
PRESSURE INFUSER received FDA 510(k) clearance on 1992-01-09, under 510(k) number K913751.
Who is the listed applicant for PRESSURE INFUSER?
The FDA 510(k) record lists Biomedical Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRESSURE INFUSER?
The FDA product code for PRESSURE INFUSER is KZD.
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 Biomedical Dynamics, 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: KZD)
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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