COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT
K-Number: K884235 · 1990-03-06
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Device Summary
Frequently Asked Questions
What is the COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT?
COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT is a medical device that received FDA 510(k) clearance on 1990-03-06. The listed applicant is Burron Medical, Inc.. The 510(k) number is K884235.
When did COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT receive FDA 510(k) clearance?
COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT received FDA 510(k) clearance on 1990-03-06, under 510(k) number K884235.
Who is the listed applicant for COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT?
The FDA 510(k) record lists Burron Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT?
The FDA product code for COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT is DRS.
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 Burron 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: DRS)
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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