Last synced on 20 May 2022 at 11:05 pm

STIMPEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822139
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1982
Days to Decision
56 days

STIMPEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822139
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1982
Days to Decision
56 days