# K962538: Bard Coagulating Resector Model (3552XX; XX=01,02,03,04,05 or 06)

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Dec 17, 1996 after 172 days
- Product code: FAS (Electrode, Electrosurgical, Active, Urological)
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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) Microvasive® (Boston Scientific Corporation) Wedge™ Electrosurgical Resection Device: named in the summary without a submission number
- (no number) CIRCON ACMI Right Angle Cutting Loop Electrode: named in the summary without a submission number

## Indications for use
The Bard Coagulating Resector is indicated for resection and coagulation of soft tissue and is intended for use with compatible resectoscopes.

Source page: https://510kreport.com/device/K962538
Methodology: https://510kreport.com/methodology