SORVALL EMBEDDING MEDIUM— 510(k) K760602

Name: FDA 510(k) clearance K760602
Creator: U.S. Food and Drug Administration
Published: 1976-09-21

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K760602 for SORVALL EMBEDDING MEDIUM, Substantially Equivalent on 1976-09-21. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: 1.

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code KEO
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1976-09-07
Decision date: 1976-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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