TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT
K-Number: K061573 · 2006-09-19
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Device Summary
Frequently Asked Questions
What is the TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT?
TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT is a medical device that received FDA 510(k) clearance on 2006-09-19. The listed applicant is Hospira, Inc.. The 510(k) number is K061573.
When did TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT receive FDA 510(k) clearance?
TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT received FDA 510(k) clearance on 2006-09-19, under 510(k) number K061573.
Who is the listed applicant for TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT?
The FDA 510(k) record lists Hospira, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT?
The FDA product code for TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND 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 Hospira, 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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