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FDA 510(k)

DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212

K-Number: K912119 · 1991-08-07

ApplicantA&D Engineering, Inc.
Decision Date1991-08-07
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212 is the device name listed in this FDA 510(k) record. The listed applicant is A&D Engineering, Inc.. It received FDA 510(k) clearance on 1991-08-07 under 510(k) number K912119. 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 DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212?

DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212 is a medical device that received FDA 510(k) clearance on 1991-08-07. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K912119.

When did DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212 receive FDA 510(k) clearance?

DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212 received FDA 510(k) clearance on 1991-08-07, under 510(k) number K912119.

Who is the listed applicant for DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212?

The FDA 510(k) record lists A&D Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212?

The FDA product code for DIGITAL SPHYGMOMANOMETER MODEL UB-211 AND 212 is DXN.

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Related Devices (Code: 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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