# K983897: Cervical Anesthesia Needle, Contracervical Anesthesia Needle, Model #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G

- Pathway: 510(k) (Traditional)
- Applicant: Ri Mos. S.R.L.
- Decided: Feb 1, 1999 after 90 days
- Product code: HEE (Set, Anesthesia, Paracervical)
- Device class: 2
- Regulation: 21 CFR 884.5100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Potocky Needle®: named in the summary without a submission number

## Indications for use
The RI. MOS. Cervical and Intracervical Anaesthesia Needles are used to apply cervical and intracervical anesthesia block.

Source page: https://510kreport.com/device/K983897
Methodology: https://510kreport.com/methodology