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ELECTRONEURAL STIMULATOR 12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831487
510(k) Type
Traditional
Applicant
MERIDIA 12 CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1983
Days to Decision
171 days

ELECTRONEURAL STIMULATOR 12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831487
510(k) Type
Traditional
Applicant
MERIDIA 12 CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1983
Days to Decision
171 days