Last synced on 14 November 2025 at 11:06 pm

STIMPEN

Page Type
Cleared 510(K)
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)
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