Last synced on 14 November 2025 at 11:06 pm

CERVICAL BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K883867
510(k) Type
Traditional
Applicant
MEND TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1988
Days to Decision
77 days

CERVICAL BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K883867
510(k) Type
Traditional
Applicant
MEND TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1988
Days to Decision
77 days