Last synced on 20 January 2023 at 11:05 pm

BIOFEEDBACK-TRAINING INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830529
510(k) Type
Traditional
Applicant
RELAXOMAT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
34 days

BIOFEEDBACK-TRAINING INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830529
510(k) Type
Traditional
Applicant
RELAXOMAT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
34 days