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FDA 510(k)

SIREDOC 60 AND SIREDOC 220

K-Number: K863331 · 1986-10-06

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1986-10-06
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIREDOC 60 AND SIREDOC 220 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 1986-10-06 under 510(k) number K863331. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIREDOC 60 AND SIREDOC 220?

SIREDOC 60 AND SIREDOC 220 is a medical device that received FDA 510(k) clearance on 1986-10-06. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K863331.

When did SIREDOC 60 AND SIREDOC 220 receive FDA 510(k) clearance?

SIREDOC 60 AND SIREDOC 220 received FDA 510(k) clearance on 1986-10-06, under 510(k) number K863331.

Who is the listed applicant for SIREDOC 60 AND SIREDOC 220?

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 SIREDOC 60 AND SIREDOC 220?

The FDA product code for SIREDOC 60 AND SIREDOC 220 is DSF.

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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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