BREWER COMPANY TEDDY CRIB MODEL 71900-A, B, 71910-A, B— 510(k) K950051

Name: FDA 510(k) clearance K950051
Creator: U.S. Food and Drug Administration
Published: 1995-02-10

Substantially Equivalent

The Brewer Co.

FDA 510(k) clearance K950051 for BREWER COMPANY TEDDY CRIB MODEL 71900-A, B, 71910-A, B, Substantially Equivalent on 1995-02-10. Applicant: The Brewer Co.. Device class: 2.

Clearance details

Applicant: The Brewer Co.
Product code: Code FMS
Device class: Class 2
Regulation: 21 CFR 880.5140
Advisory panel: General Hospital
Date received: 1995-01-06
Decision date: 1995-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menomonee Falls, WI, US

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