510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884924Substantially Equivalent

Visi-Wipe

Visitec Co., Sarasota FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884924 is the FDA 510(k) clearance record for VISI-WIPE, a class I device, cleared for Visitec Co. on under FDA product code HOF (Burr, Corneal, Manual). FDA records list 49 510(k) clearances for Visitec Co., from to . As of , FDA records show no recalls naming K884924.

Clearance record

Decision date
Received
(64 days to decision)
Product code
HOF Burr, Corneal, Manual
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Applicant
Visitec Co. 7575 Commerce Ct., Sarasota FL
Third party review
No

Clearances, product code HOF

Trailing 12 months

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

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