DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)— 510(k) K960400

Name: FDA 510(k) clearance K960400
Creator: U.S. Food and Drug Administration
Published: 1996-03-12

Substantially Equivalent

Snowden-Pencer

FDA 510(k) clearance K960400 for DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS), Substantially Equivalent on 1996-03-12. Applicant: Snowden-Pencer. Device class: 1.

Clearance details

Applicant: Snowden-Pencer
Product code: Code FBM
Device class: Class 1
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1996-01-29
Decision date: 1996-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucker, GA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.