TUMBLER, GENERAL MEDICAL MEDI-PAK— 510(k) K760491

Name: FDA 510(k) clearance K760491
Creator: U.S. Food and Drug Administration
Published: 1976-09-15

Substantially Equivalent

Landmark Plastics

FDA 510(k) clearance K760491 for TUMBLER, GENERAL MEDICAL MEDI-PAK, Substantially Equivalent on 1976-09-15. Applicant: Landmark Plastics. Device class: 2.

Clearance details

Applicant: Landmark Plastics
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1976-08-23
Decision date: 1976-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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