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FDA 510(k)

DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A

K-Number: K883359 · 1989-01-25

ApplicantToshiba Medical Systems
Decision Date1989-01-25
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1989-01-25 under 510(k) number K883359. 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 DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A?

DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A is a medical device that received FDA 510(k) clearance on 1989-01-25. The listed applicant is Toshiba Medical Systems. The 510(k) number is K883359.

When did DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A receive FDA 510(k) clearance?

DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A received FDA 510(k) clearance on 1989-01-25, under 510(k) number K883359.

Who is the listed applicant for DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A?

The FDA 510(k) record lists Toshiba Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A?

The FDA product code for DIAGNOSTIC ULTRASOUND SYSTEM SSA-270A is IYO.

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Other records listing Toshiba Medical Systems 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.

K960948SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020AK954310BLA-800AK954309ANGIOREXK893750MRT-50A MOBILEK891453DIAGNOSTIC ULTRASOUND TRANSDUCER: PVE-582VK890969TRANSESOPHAGEAL TRANSDUCER PEF-511SA

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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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