# K060320: Femecc Endocervical Curette

- Pathway: 510(k) (Traditional)
- Applicant: Femspec LLC
- Decided: Jul 28, 2006 after 170 days
- Product code: PCF (Sampler, Endocervical)
- Device class: 2
- Regulation: 21 CFR 884.1050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K122658: Femcerv Endocervical Sampler Model 3 Sizes: Ref FCV-013, Ref FCV-011, Ref FCV-009 (2012), 0 descendants of its own

## Indications for use
FemSpec, LLC, FemECC™ Endocervical Curette is a sterile, disposable curette indicated for single patient use in obtaining tissue samples from the endocervical canal for histological analysis.

Source page: https://510kreport.com/device/K060320
Methodology: https://510kreport.com/methodology