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FDA 510(k)

ELECTRONIC BLOOD PRESSURE UNIT

K-Number: K761302 · 1977-01-05

ApplicantMedline Industries, Inc.
Decision Date1977-01-05
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC BLOOD PRESSURE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761302. 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 ELECTRONIC BLOOD PRESSURE UNIT?

ELECTRONIC BLOOD PRESSURE UNIT is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Medline Industries, Inc.. The 510(k) number is K761302.

When did ELECTRONIC BLOOD PRESSURE UNIT receive FDA 510(k) clearance?

ELECTRONIC BLOOD PRESSURE UNIT received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761302.

Who is the listed applicant for ELECTRONIC BLOOD PRESSURE UNIT?

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

What is the FDA product code for ELECTRONIC BLOOD PRESSURE UNIT?

The FDA product code for ELECTRONIC BLOOD PRESSURE UNIT is DXN.

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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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