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)

CATHETERIZATION C-ARM SUPPORT MH-51B(F)

K-Number: K903371 · 1990-11-29

Decision Date1990-11-29
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CATHETERIZATION C-ARM SUPPORT MH-51B(F) is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1990-11-29 under 510(k) number K903371. 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 CATHETERIZATION C-ARM SUPPORT MH-51B(F)?

CATHETERIZATION C-ARM SUPPORT MH-51B(F) is a medical device that received FDA 510(k) clearance on 1990-11-29. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K903371.

When did CATHETERIZATION C-ARM SUPPORT MH-51B(F) receive FDA 510(k) clearance?

CATHETERIZATION C-ARM SUPPORT MH-51B(F) received FDA 510(k) clearance on 1990-11-29, under 510(k) number K903371.

Who is the listed applicant for CATHETERIZATION C-ARM SUPPORT MH-51B(F)?

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

What is the FDA product code for CATHETERIZATION C-ARM SUPPORT MH-51B(F)?

The FDA product code for CATHETERIZATION C-ARM SUPPORT MH-51B(F) 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 Shimadzu Medical Systems 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 90 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.

↑