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)

COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF

K-Number: K862151 · 1986-09-19

Decision Date1986-09-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1986-09-19 under 510(k) number K862151. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF?

COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF is a medical device that received FDA 510(k) clearance on 1986-09-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K862151.

When did COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF receive FDA 510(k) clearance?

COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF received FDA 510(k) clearance on 1986-09-19, under 510(k) number K862151.

Who is the listed applicant for COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF?

The FDA product code for COLOR FLOW MAPPING (CFM) OPTION - MODEL 77020 CF is IYO.

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 Hewlett-Packard Co. 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.

View all 230 devices →

Related Devices (Code: IYO)

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.

↑