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Ear Curette

by Ear Tech, Inc.

510(k) K932609

Ear Curette is a medical device (FDA Class I; FDA product code JYG, Curette, Ear) made by Ear Tech, Inc., cleared under FDA 510(k) K932609 on 21 Jul 1993, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK932609 Date21 Jul 1993ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JYG
Device class
Class I
Regulation
21 CFR Part 874.4420
Advisory committee
Ear, Nose, Throat
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code JYG (Curette, Ear).

Other devices from Ear Tech, Inc.