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FDA 510(k)

5.0 MHZ INTRAOPERATIVE ARRAY

K-Number: K860123 · 1986-07-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1986-07-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

5.0 MHZ INTRAOPERATIVE ARRAY 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 1986-07-07 under 510(k) number K860123. 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 INTRAOPERATIVE ARRAY?

5.0 MHZ INTRAOPERATIVE ARRAY is a medical device that received FDA 510(k) clearance on 1986-07-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K860123.

When did 5.0 MHZ INTRAOPERATIVE ARRAY receive FDA 510(k) clearance?

5.0 MHZ INTRAOPERATIVE ARRAY received FDA 510(k) clearance on 1986-07-07, under 510(k) number K860123.

Who is the listed applicant for 5.0 MHZ INTRAOPERATIVE ARRAY?

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 INTRAOPERATIVE ARRAY?

The FDA product code for 5.0 MHZ INTRAOPERATIVE ARRAY 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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