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FDA 510(k)

SIREDOC, PAPER CHART RECORDER

K-Number: K850146 · 1985-02-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1985-02-12
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIREDOC, PAPER CHART RECORDER 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 1985-02-12 under 510(k) number K850146. 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, PAPER CHART RECORDER?

SIREDOC, PAPER CHART RECORDER is a medical device that received FDA 510(k) clearance on 1985-02-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K850146.

When did SIREDOC, PAPER CHART RECORDER receive FDA 510(k) clearance?

SIREDOC, PAPER CHART RECORDER received FDA 510(k) clearance on 1985-02-12, under 510(k) number K850146.

Who is the listed applicant for SIREDOC, PAPER CHART RECORDER?

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, PAPER CHART RECORDER?

The FDA product code for SIREDOC, PAPER CHART RECORDER 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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