# K951529: V. Mueller Obstetrical (OB) Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Aug 4, 1995 after 123 days
- Product code: HDA (Forceps, Obstetrical)
- Device class: 2
- Regulation: 21 CFR 884.4400
- 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
- K013747: Tekno-Medical Obstetrical Forceps (2002), 2 descendants of its own
- K100517: Instrumed Forceps Obsterical, Model# 46-5XXX, OB-XXXX (2010), 0 descendants of its own
- K092827: Dimela Obsterical Forceps, Model 72.1 XX XX (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K951529
Methodology: https://510kreport.com/methodology