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VERSION 4.2 APPLICATION SOFTWARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892959
510(k) Type
Traditional
Applicant
RESONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1989
Days to Decision
38 days