510(k) K882606

EURO-MED ENDO-CURETTE by Buckman Co., Inc. — Product Code PCF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 25, 1988
Date Received
June 24, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sampler, Endocervical
Device Class
Class II
Regulation Number
884.1050
Review Panel
OB
Submission Type

Obtains tissue samples from the endocervical canal for histological analysis.