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)

MAGNI-CAM

K-Number: K920069 · 1992-03-02

ApplicantInnoventions, Inc.
Decision Date1992-03-02
Product CodeHJG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MAGNI-CAM is the device name listed in this FDA 510(k) record. The listed applicant is Innoventions, Inc.. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K920069. The device is classified under product code HJG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNI-CAM?

MAGNI-CAM is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Innoventions, Inc.. The 510(k) number is K920069.

When did MAGNI-CAM receive FDA 510(k) clearance?

MAGNI-CAM received FDA 510(k) clearance on 1992-03-02, under 510(k) number K920069.

Who is the listed applicant for MAGNI-CAM?

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

What is the FDA product code for MAGNI-CAM?

The FDA product code for MAGNI-CAM is HJG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: HJG)

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.

K933633LOW-VISION READING AID, HELPMATE 2020, VISION-AIDE, LV HELPMATEGracefully Yours, Inc.K915340MENTOR HORIZON LOW VISION MAGNIFIERMentor O & O, Inc.K892351MAGNILINK SYSTEM 602Coburn Optical Ind., Inc.K892350MAGNILINK SYSTEM 402/5Coburn Optical Ind., Inc.K892347MAGNILINK SYSTEM 101Coburn Optical Ind., Inc.K892348MAGNILINK SYSTEM 201Coburn Optical Ind., Inc.

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.

↑