Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DIGITAL SPHGMOMANOMETER UA-271

K-Number: K832723 · 1984-04-17

ApplicantCopal, Inc.
Decision Date1984-04-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL SPHGMOMANOMETER UA-271 is the device name listed in this FDA 510(k) record. The listed applicant is Copal, Inc.. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K832723. 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 SPHGMOMANOMETER UA-271?

DIGITAL SPHGMOMANOMETER UA-271 is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Copal, Inc.. The 510(k) number is K832723.

When did DIGITAL SPHGMOMANOMETER UA-271 receive FDA 510(k) clearance?

DIGITAL SPHGMOMANOMETER UA-271 received FDA 510(k) clearance on 1984-04-17, under 510(k) number K832723.

Who is the listed applicant for DIGITAL SPHGMOMANOMETER UA-271?

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

What is the FDA product code for DIGITAL SPHGMOMANOMETER UA-271?

The FDA product code for DIGITAL SPHGMOMANOMETER UA-271 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.

Other records listing Copal, 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.

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.

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.

↑