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FDA 510(k)

MODIFIED DRAGER SPHYGMOMED

K-Number: K862427 · 1987-03-23

ApplicantDraeger Medical, Inc.
Decision Date1987-03-23
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED DRAGER SPHYGMOMED 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 1987-03-23 under 510(k) number K862427. 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 DRAGER SPHYGMOMED?

MODIFIED DRAGER SPHYGMOMED is a medical device that received FDA 510(k) clearance on 1987-03-23. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K862427.

When did MODIFIED DRAGER SPHYGMOMED receive FDA 510(k) clearance?

MODIFIED DRAGER SPHYGMOMED received FDA 510(k) clearance on 1987-03-23, under 510(k) number K862427.

Who is the listed applicant for MODIFIED DRAGER SPHYGMOMED?

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 DRAGER SPHYGMOMED?

The FDA product code for MODIFIED DRAGER SPHYGMOMED is DXN.

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Other records listing Draeger Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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