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FDA 510(k)

MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT

K-Number: K871886 · 1987-07-29

ApplicantDraeger Medical, Inc.
Decision Date1987-07-29
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1987-07-29 under 510(k) number K871886. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT?

MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT is a medical device that received FDA 510(k) clearance on 1987-07-29. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K871886.

When did MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT receive FDA 510(k) clearance?

MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT received FDA 510(k) clearance on 1987-07-29, under 510(k) number K871886.

Who is the listed applicant for MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT?

The FDA 510(k) record lists Draeger Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT?

The FDA product code for MODIFIED SPHYGMOMED NON-INVASIVE BLOOD PRES. MONIT is DXN.

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Other records listing Draeger Medical, Inc. as applicant

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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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