FDA 510(k)

H-O CAMERA

K-Number: K831832 · 1983-07-07

Decision Date1983-07-07

Product Code

DecisionSubstantially Equivalent

Device Summary

H-O CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Uni-Quatro Industries. It received FDA 510(k) clearance on 1983-07-07 under 510(k) number K831832. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H-O CAMERA?

H-O CAMERA is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Uni-Quatro Industries. The 510(k) number is K831832.

When did H-O CAMERA receive FDA 510(k) clearance?

H-O CAMERA received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831832.

Who is the listed applicant for H-O CAMERA?

The FDA 510(k) record lists Uni-Quatro Industries 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Uni-Quatro Industries as applicant

K863856S-RAY CAMERA K831833MX CAMERA

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.