510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K932259Substantially Equivalent

Clarus Model 2240 Semi-Rigid Otoscope

Clarus Medical Systems, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932259 is the FDA 510(k) clearance record for CLARUS MODEL 2240 SEMI-RIGID OTOSCOPE, a class I device, cleared for Clarus Medical Systems, Inc. on under FDA product code ERA (Otoscope). FDA records list 22 510(k) clearances for Clarus Medical Systems, Inc., from to . As of , FDA records show no recalls naming K932259.

Clearance record

Decision date
Received
(239 days to decision)
Product code
ERA Otoscope
Regulation
21 CFR 874.4770
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Clarus Medical Systems, Inc. 2605 Fernbrook La, Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code ERA

Trailing 12 months

FDA records hold no clearances under product code ERA in the trailing twelve months.

FDA records show no clearances under product code ERA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ERA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260