510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K820889Substantially Equivalent

Aspirator/irrigator or I/a Unit

Mid Laboratories, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820889 is the FDA 510(k) clearance record for ASPIRATOR/IRRIGATOR OR I/A UNIT, a class I device, cleared for Mid Laboratories, Inc. on under FDA product code KYG (Device, Irrigation, Ocular Surgery). FDA records list 2 510(k) clearances for Mid Laboratories, Inc., from to . As of , FDA records show no recalls naming K820889.

Clearance record

Decision date
Received
(36 days to decision)
Product code
KYG Device, Irrigation, Ocular Surgery
Regulation
21 CFR 886.4360
Device class
Class I
Review panel
Ophthalmic
Applicant
Mid Laboratories, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KYG

Trailing 12 months

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

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