# K842112: Tischler Cervical Biopsy Punch Forceps

- Pathway: 510(k) (Traditional)
- Applicant: J. Sklar Mfg. Co., Inc.
- Decided: Jul 3, 1984 after 35 days
- Product code: HFB (Forceps, Biopsy, Gynecological)
- Device class: 1
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K080095: Coramate/Spirotome System (2008), 1 descendant of its own
- K190378: Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K842112
Methodology: https://510kreport.com/methodology