L.T.C. REPLACEMENT GASTROSTOMY TUBE— 510(k) K896621

Name: FDA 510(k) clearance K896621
Creator: U.S. Food and Drug Administration
Published: 1990-03-13

Substantially Equivalent

Intl. Medical Marketing, Inc.

FDA 510(k) clearance K896621 for L.T.C. REPLACEMENT GASTROSTOMY TUBE, Substantially Equivalent on 1990-03-13. Applicant: Intl. Medical Marketing, Inc.. Device class: 1.

Clearance details

Applicant: Intl. Medical Marketing, Inc.
Product code: Code KCQ
Device class: Class 1
Regulation: 21 CFR 872.6570
Advisory panel: Dental
Date received: 1989-11-21
Decision date: 1990-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ridge, NY, US

Download summary PDF View on FDA.gov ↗

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