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ECG-GEL ELECTRODE GEL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833172
510(k) Type
Traditional
Applicant
WHS PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1983
Days to Decision
66 days

ECG-GEL ELECTRODE GEL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833172
510(k) Type
Traditional
Applicant
WHS PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1983
Days to Decision
66 days