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)

NAMIC CONTRAST SAVINGS DELIVERY SYSTEM

K-Number: K903493 · 1991-03-26

Decision Date1991-03-26
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NAMIC CONTRAST SAVINGS DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1991-03-26 under 510(k) number K903493. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMIC CONTRAST SAVINGS DELIVERY SYSTEM?

NAMIC CONTRAST SAVINGS DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1991-03-26. The listed applicant is North American Instrument Corp.. The 510(k) number is K903493.

When did NAMIC CONTRAST SAVINGS DELIVERY SYSTEM receive FDA 510(k) clearance?

NAMIC CONTRAST SAVINGS DELIVERY SYSTEM received FDA 510(k) clearance on 1991-03-26, under 510(k) number K903493.

Who is the listed applicant for NAMIC CONTRAST SAVINGS DELIVERY SYSTEM?

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

What is the FDA product code for NAMIC CONTRAST SAVINGS DELIVERY SYSTEM?

The FDA product code for NAMIC CONTRAST SAVINGS DELIVERY SYSTEM is IZI.

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 North American Instrument 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.

View all 28 devices →

Related Devices (Code: IZI)

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.

↑