TUBE, HEAVY GLASS WALL INJECTION— 510(k) K760500

Name: FDA 510(k) clearance K760500
Creator: U.S. Food and Drug Administration
Published: 1976-09-03

Substantially Equivalent

Unimetrics Corp.

FDA 510(k) clearance K760500 for TUBE, HEAVY GLASS WALL INJECTION, Substantially Equivalent on 1976-09-03. Applicant: Unimetrics Corp.. Device class: 2.

Clearance details

Applicant: Unimetrics Corp.
Product code: Code DXL
Device class: Class 2
Regulation: 21 CFR 870.1660
Advisory panel: Cardiovascular
Date received: 1976-08-23
Decision date: 1976-09-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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