# K990366: Exmoor Suction Clearance Kit

- Pathway: 510(k) (Traditional)
- Applicant: Exmoor Plastics, Ltd.
- Decided: Mar 5, 1999 after 28 days
- Product code: LRC (Instrument, Ent Manual Surgical)
- Device class: 1
- Regulation: 21 CFR 874.4420
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K973587 (1998). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K973587: Exmoor Tympanocentesis Kit (TK/1), Exmoor Plastics, Ltd. (1998) Summary page 1.
- K980828: Exmoor Myringotomy Kit, Exmoor Plastics, Ltd. (1998) Summary page 1.
- (no number) Richards Ear Examkit: named in the summary without a submission number

## Indications for use
The need to clear and clean the external ear canal.

Source page: https://510kreport.com/device/K990366
Methodology: https://510kreport.com/methodology