# K910252: Potocky Neddle (TM) Disposable Injection Needle

- Pathway: 510(k) (Traditional)
- Applicant: CooperSurgical, Inc.
- Decided: Mar 4, 1991 after 41 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021224: Endocervical Block Needle (2002), 1 descendant of its own
- K052365: Cervineedle Disposable Cartridge Syringe (2005), 0 descendants of its own
- K980238: Gynex Extended Reach Needle (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K910252
Methodology: https://510kreport.com/methodology