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FDA 510(k)

TYPE 9541 RECORDER, PAPER CHART

K-Number: K895111 · 1990-01-26

ApplicantS & W Medico Teknik
Decision Date1990-01-26
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TYPE 9541 RECORDER, PAPER CHART is the device name listed in this FDA 510(k) record. The listed applicant is S & W Medico Teknik. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K895111. 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 TYPE 9541 RECORDER, PAPER CHART?

TYPE 9541 RECORDER, PAPER CHART is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is S & W Medico Teknik. The 510(k) number is K895111.

When did TYPE 9541 RECORDER, PAPER CHART receive FDA 510(k) clearance?

TYPE 9541 RECORDER, PAPER CHART received FDA 510(k) clearance on 1990-01-26, under 510(k) number K895111.

Who is the listed applicant for TYPE 9541 RECORDER, PAPER CHART?

The FDA 510(k) record lists S & W Medico Teknik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYPE 9541 RECORDER, PAPER CHART?

The FDA product code for TYPE 9541 RECORDER, PAPER CHART is DSF.

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Other records listing S & W Medico Teknik as applicant

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Related Devices (Code: 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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