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)

ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG

K-Number: K954282 · 1996-02-06

Decision Date1996-02-06
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG is the device name listed in this FDA 510(k) record. The listed applicant is Statcorp, Inc.. It received FDA 510(k) clearance on 1996-02-06 under 510(k) number K954282. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG?

ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG is a medical device that received FDA 510(k) clearance on 1996-02-06. The listed applicant is Statcorp, Inc.. The 510(k) number is K954282.

When did ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG receive FDA 510(k) clearance?

ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG received FDA 510(k) clearance on 1996-02-06, under 510(k) number K954282.

Who is the listed applicant for ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG?

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

What is the FDA product code for ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG?

The FDA product code for ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG is DXQ.

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 Statcorp, 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: DXQ)

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.

↑