# K984607: Panoview Plus Optic with 2.7MM Diameter, Model 8672.XXX, Panoview Plus Optic with 1.9MM Diameter, Model 8686.XXX

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Mar 5, 1999 after 67 days
- Product code: FBP (Telescope, Rigid, Endoscopic)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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) Cysto-Urethrosocpe for children, Model 8670 and 8680: named in the summary without a submission number

## Indications for use
The endoscopes serve to visualize the inside of the patient via natural or surgically generated access. For examination, diagnosis and/or therapy by personnel trained in the use of endoscopic instrumentation used in various medical disciplines, such as surgery, urology, gynecology, and ENT.

Source page: https://510kreport.com/device/K984607
Methodology: https://510kreport.com/methodology