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FDA 510(k)

ANEROID BLOOD PRESSURE GAUGE

K-Number: K904376 · 1990-12-20

ApplicantBiomedical Dynamics, Inc.
Decision Date1990-12-20
Product CodeFCY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANEROID BLOOD PRESSURE GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Dynamics, Inc.. It received FDA 510(k) clearance on 1990-12-20 under 510(k) number K904376. The device is classified under product code FCY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEROID BLOOD PRESSURE GAUGE?

ANEROID BLOOD PRESSURE GAUGE is a medical device that received FDA 510(k) clearance on 1990-12-20. The listed applicant is Biomedical Dynamics, Inc.. The 510(k) number is K904376.

When did ANEROID BLOOD PRESSURE GAUGE receive FDA 510(k) clearance?

ANEROID BLOOD PRESSURE GAUGE received FDA 510(k) clearance on 1990-12-20, under 510(k) number K904376.

Who is the listed applicant for ANEROID BLOOD PRESSURE GAUGE?

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

What is the FDA product code for ANEROID BLOOD PRESSURE GAUGE?

The FDA product code for ANEROID BLOOD PRESSURE GAUGE is FCY.

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Other records listing Biomedical Dynamics, 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.

K915074IRRIGATOR/ASPIRATOR PROBEK913751PRESSURE INFUSERK911213CUFFABLEK911216INFUSABLEK911324IRRIGATION/ASPIRATION TUBING SETK890268PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION

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Related Devices (Code: FCY)

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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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