Last synced on 6 June 2025 at 11:06 pm

ELECTRICAL MUSCLE STIMULATOR DEVICE ( PGS-4000)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980346
510(k) Type
Traditional
Applicant
UNIVERSAL TECHNOLOGY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1998
Days to Decision
90 days
Submission Type
Statement

ELECTRICAL MUSCLE STIMULATOR DEVICE ( PGS-4000)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980346
510(k) Type
Traditional
Applicant
UNIVERSAL TECHNOLOGY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1998
Days to Decision
90 days
Submission Type
Statement