BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE
K-Number: K061932 · 2006-09-14
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Device Summary
Frequently Asked Questions
What is the BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE?
BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE is a medical device that received FDA 510(k) clearance on 2006-09-14. The listed applicant is Cardiopulmonary Corp.. The 510(k) number is K061932.
When did BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE receive FDA 510(k) clearance?
BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE received FDA 510(k) clearance on 2006-09-14, under 510(k) number K061932.
Who is the listed applicant for BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE?
The FDA 510(k) record lists Cardiopulmonary Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE?
The FDA product code for BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE is MSX.
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 Cardiopulmonary Corp. 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: MSX)
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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