Last synced on 30 September 2022 at 11:05 pm

KOLPLAST VAGINAL SPECULUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973853
510(k) Type
Traditional
Applicant
KOLPLAST COMERCIAL E INDUSTRIAL LTDA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
72 days
Submission Type
Statement

KOLPLAST VAGINAL SPECULUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973853
510(k) Type
Traditional
Applicant
KOLPLAST COMERCIAL E INDUSTRIAL LTDA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1997
Days to Decision
72 days
Submission Type
Statement