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)

MULTI-VIEW PROCESSOR (MVP)

K-Number: K931184 · 1993-11-02

Decision Date1993-11-02
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI-VIEW PROCESSOR (MVP) is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K931184. 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 MULTI-VIEW PROCESSOR (MVP)?

MULTI-VIEW PROCESSOR (MVP) is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Adac Laboratories. The 510(k) number is K931184.

When did MULTI-VIEW PROCESSOR (MVP) receive FDA 510(k) clearance?

MULTI-VIEW PROCESSOR (MVP) received FDA 510(k) clearance on 1993-11-02, under 510(k) number K931184.

Who is the listed applicant for MULTI-VIEW PROCESSOR (MVP)?

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

What is the FDA product code for MULTI-VIEW PROCESSOR (MVP)?

The FDA product code for MULTI-VIEW PROCESSOR (MVP) 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 Adac Laboratories 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 88 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.

↑