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GOLD CD ULTRA MINI CANAL - MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951642
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1995
Days to Decision
92 days
Submission Type
Statement