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FDA 510(k)

AIDA DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K103148 · 2011-03-11

ApplicantPanasonic Healthcare Co., Ltd.
Decision Date2011-03-11
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AIDA DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Healthcare Co., Ltd.. It received FDA 510(k) clearance on 2011-03-11 under 510(k) number K103148. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIDA DIAGNOSTIC ULTRASOUND SYSTEM?

AIDA DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2011-03-11. The listed applicant is Panasonic Healthcare Co., Ltd.. The 510(k) number is K103148.

When did AIDA DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

AIDA DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 2011-03-11, under 510(k) number K103148.

Who is the listed applicant for AIDA DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA 510(k) record lists Panasonic Healthcare Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIDA DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for AIDA DIAGNOSTIC ULTRASOUND SYSTEM is IYO.

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Other records listing Panasonic Healthcare Co., Ltd. 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.

K122009AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCERK113612AIDA V1.5 DIAGNOSTIC ULTRASOUND SYSTEM GM-72P00A

Related Devices (Code: IYO)

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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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