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INTRAUTERINE DEVICE REMOVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842295
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1984
Days to Decision
123 days

INTRAUTERINE DEVICE REMOVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842295
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1984
Days to Decision
123 days