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)

TUBE, HEAVY GLASS WALL INJECTION

K-Number: K760500 · 1976-09-03

ApplicantUnimetrics Corp.
Decision Date1976-09-03
Product CodeDXL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TUBE, HEAVY GLASS WALL INJECTION is the device name listed in this FDA 510(k) record. The listed applicant is Unimetrics Corp.. It received FDA 510(k) clearance on 1976-09-03 under 510(k) number K760500. The device is classified under product code DXL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE, HEAVY GLASS WALL INJECTION?

TUBE, HEAVY GLASS WALL INJECTION is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Unimetrics Corp.. The 510(k) number is K760500.

When did TUBE, HEAVY GLASS WALL INJECTION receive FDA 510(k) clearance?

TUBE, HEAVY GLASS WALL INJECTION received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760500.

Who is the listed applicant for TUBE, HEAVY GLASS WALL INJECTION?

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

What is the FDA product code for TUBE, HEAVY GLASS WALL INJECTION?

The FDA product code for TUBE, HEAVY GLASS WALL INJECTION is DXL.

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 Unimetrics Corp. 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.

K7705003 PORT LUER

Related Devices (Code: DXL)

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.

K760448SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECTInstrumentation Laboratory COK760066TRAY, ICED INJECTABLE (26420)Instrumentation Laboratory CO

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.

↑