Last synced on 4 February 2023 at 10:33 pm

PREMIER K-AMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914799
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1992
Days to Decision
118 days
Submission Type
Statement