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FDA 510(k)

5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517

K-Number: K852570 · 1985-09-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1985-09-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517 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 1985-09-19 under 510(k) number K852570. 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 5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517?

5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517 is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K852570.

When did 5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517 receive FDA 510(k) clearance?

5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517 received FDA 510(k) clearance on 1985-09-19, under 510(k) number K852570.

Who is the listed applicant for 5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517?

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 5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517?

The FDA product code for 5.0 MHZ LINEAR ARRAY, MODEL 83, 39, 517 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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