510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831829Substantially Equivalent

Karickhoff Flying Corpuscle Viewer

Surgidev Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831829 is the FDA 510(k) clearance record for KARICKHOFF FLYING CORPUSCLE VIEWER, a class I device, cleared for Surgidev Corp. on under FDA product code HIX (Maxwell Spot, Ac-Powered). FDA records list 4 510(k) clearances for Surgidev Corp., from to . As of , FDA records show no recalls naming K831829.

Clearance record

Decision date
Received
(134 days to decision)
Product code
HIX Maxwell Spot, Ac-Powered
Regulation
21 CFR 886.1435
Device class
Class I
Review panel
Ophthalmic
Applicant
Surgidev Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HIX

Trailing 12 months

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

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