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SURGITEK ULTRA-LO CUFF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830504
510(k) Type
Traditional
Applicant
MEC/SURGITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1983
Days to Decision
55 days

SURGITEK ULTRA-LO CUFF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830504
510(k) Type
Traditional
Applicant
MEC/SURGITEK PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1983
Days to Decision
55 days