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FDA 510(k)

AUTOMATIC ELECTRONIC SPHYGMOMANOMETER

K-Number: K760738 · 1977-01-21

ApplicantMedical Monitors, Inc.
Decision Date1977-01-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC ELECTRONIC SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Monitors, Inc.. It received FDA 510(k) clearance on 1977-01-21 under 510(k) number K760738. 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 AUTOMATIC ELECTRONIC SPHYGMOMANOMETER?

AUTOMATIC ELECTRONIC SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1977-01-21. The listed applicant is Medical Monitors, Inc.. The 510(k) number is K760738.

When did AUTOMATIC ELECTRONIC SPHYGMOMANOMETER receive FDA 510(k) clearance?

AUTOMATIC ELECTRONIC SPHYGMOMANOMETER received FDA 510(k) clearance on 1977-01-21, under 510(k) number K760738.

Who is the listed applicant for AUTOMATIC ELECTRONIC SPHYGMOMANOMETER?

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

What is the FDA product code for AUTOMATIC ELECTRONIC SPHYGMOMANOMETER?

The FDA product code for AUTOMATIC ELECTRONIC SPHYGMOMANOMETER is DXN.

Related Clinical Trials

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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Other records listing Medical Monitors, 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.

K893557ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)

Related Devices (Code: DXN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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