Last synced on 14 November 2025 at 11:06 pm

SOMATOSENSORY STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K810482
510(k) Type
Traditional
Applicant
AMPLAID USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1981
Days to Decision
65 days

SOMATOSENSORY STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K810482
510(k) Type
Traditional
Applicant
AMPLAID USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1981
Days to Decision
65 days