Last synced on 20 December 2024 at 11:05 pm

GYNE-SHEAR CERVICAL BIOPSY INSTRUMENT W/DISPIS TIP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852357
510(k) Type
Traditional
Applicant
GYNECO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1985
Days to Decision
32 days

GYNE-SHEAR CERVICAL BIOPSY INSTRUMENT W/DISPIS TIP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852357
510(k) Type
Traditional
Applicant
GYNECO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1985
Days to Decision
32 days