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SKYLARK MODEL 1001 TENS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853898
510(k) Type
Traditional
Applicant
PELEG INTL. CO.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/18/1986
Days to Decision
271 days

SKYLARK MODEL 1001 TENS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853898
510(k) Type
Traditional
Applicant
PELEG INTL. CO.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/18/1986
Days to Decision
271 days