DISPOSABLE CATHETER PRESSURE TRANSDUCER
K-Number: K874165 · 1988-06-09
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE CATHETER PRESSURE TRANSDUCER?
DISPOSABLE CATHETER PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1988-06-09. The listed applicant is Deseret Medical, Inc.. The 510(k) number is K874165.
When did DISPOSABLE CATHETER PRESSURE TRANSDUCER receive FDA 510(k) clearance?
DISPOSABLE CATHETER PRESSURE TRANSDUCER received FDA 510(k) clearance on 1988-06-09, under 510(k) number K874165.
Who is the listed applicant for DISPOSABLE CATHETER PRESSURE TRANSDUCER?
The FDA 510(k) record lists Deseret Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE CATHETER PRESSURE TRANSDUCER?
The FDA product code for DISPOSABLE CATHETER PRESSURE TRANSDUCER is DXO.
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 Deseret Medical, 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: DXO)
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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