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FDA 510(k)

SIEMENS SONOLINE AC

K-Number: K896480 · 1990-07-13

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1990-07-13
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS SONOLINE AC is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1990-07-13 under 510(k) number K896480. 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 SIEMENS SONOLINE AC?

SIEMENS SONOLINE AC is a medical device that received FDA 510(k) clearance on 1990-07-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K896480.

When did SIEMENS SONOLINE AC receive FDA 510(k) clearance?

SIEMENS SONOLINE AC received FDA 510(k) clearance on 1990-07-13, under 510(k) number K896480.

Who is the listed applicant for SIEMENS SONOLINE AC?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS SONOLINE AC?

The FDA product code for SIEMENS SONOLINE AC is 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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