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)

TYTAN BLOOD PRESSURE CUFF

K-Number: K062238 · 2006-09-21

Decision Date2006-09-21
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TYTAN BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Tytan Medical Corp.. It received FDA 510(k) clearance on 2006-09-21 under 510(k) number K062238. 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 TYTAN BLOOD PRESSURE CUFF?

TYTAN BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2006-09-21. The listed applicant is Tytan Medical Corp.. The 510(k) number is K062238.

When did TYTAN BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

TYTAN BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2006-09-21, under 510(k) number K062238.

Who is the listed applicant for TYTAN BLOOD PRESSURE CUFF?

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

What is the FDA product code for TYTAN BLOOD PRESSURE CUFF?

The FDA product code for TYTAN BLOOD PRESSURE CUFF 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 Tytan Medical Corp. 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.

↑