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)

CAMERAS, MULTI-IMAGE

K-Number: K781214 · 1978-09-14

ApplicantDunn Instruments, Inc.
Decision Date1978-09-14
Product Code
DecisionSubstantially Equivalent

Device Summary

CAMERAS, MULTI-IMAGE is the device name listed in this FDA 510(k) record. The listed applicant is Dunn Instruments, Inc.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781214. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMERAS, MULTI-IMAGE?

CAMERAS, MULTI-IMAGE is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Dunn Instruments, Inc.. The 510(k) number is K781214.

When did CAMERAS, MULTI-IMAGE receive FDA 510(k) clearance?

CAMERAS, MULTI-IMAGE received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781214.

Who is the listed applicant for CAMERAS, MULTI-IMAGE?

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

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

Other records listing Dunn Instruments, Inc. 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.

K850184MEDICAL MULTI-IMAGE CAMERA-676K771924HEARTBEATER

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.

↑