WAYMOUTH'S POWDER MEDIUM— 510(k) K821917

Name: FDA 510(k) clearance K821917
Creator: U.S. Food and Drug Administration
Published: 1982-07-27

Substantially Equivalent

Dutchland Laboratories, Inc.

FDA 510(k) clearance K821917 for WAYMOUTH'S POWDER MEDIUM, Substantially Equivalent on 1982-07-27. Applicant: Dutchland Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Dutchland Laboratories, Inc.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1982-06-28
Decision date: 1982-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dutchland Laboratories, Inc.

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K821911 — S-MEM-JOKLIK'S POWDER1982-07-27
K821912 — MCCOY'S POWDER MEDIUM 5A SUSPENSION1982-07-27
K821913 — ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM1982-07-27
K821914 — COON'S F-12 POWDER MEDIUM1982-07-27
K821915 — BME AUTOCLAVABLE MEDIUM1982-07-27

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