510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K802279Substantially Equivalent

Vida 55 Pulse-Echo Ultrasonic Device

Vida, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802279 is the FDA 510(k) clearance record for VIDA 55 PULSE-ECHO ULTRASONIC DEVICE, a class II device, cleared for Vida, Inc. on under FDA product code EWG (Laser, Ent Microsurgical Carbon-Dioxide). FDA records list one 510(k) clearance for Vida, Inc. As of , FDA records show no recalls naming K802279.

Clearance record

Decision date
Received
(88 days to decision)
Product code
EWG Laser, Ent Microsurgical Carbon-Dioxide
Regulation
21 CFR 874.4500
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Vida, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EWG

Trailing 12 months

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

FDA records show no clearances under product code EWG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EWG, 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