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FDA 510(k)

DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)

K-Number: K052828 · 2006-02-17

ApplicantHospira, Inc.
Decision Date2006-02-17
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT) is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2006-02-17 under 510(k) number K052828. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)?

DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT) is a medical device that received FDA 510(k) clearance on 2006-02-17. The listed applicant is Hospira, Inc.. The 510(k) number is K052828.

When did DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT) receive FDA 510(k) clearance?

DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT) received FDA 510(k) clearance on 2006-02-17, under 510(k) number K052828.

Who is the listed applicant for DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)?

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 DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)?

The FDA product code for DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT) 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.

View all 36 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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