510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863775Substantially Equivalent

Rk Vacuum Fixation Ring System

Ameritek, Inc., Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863775 is the FDA 510(k) clearance record for RK VACUUM FIXATION RING SYSTEM, a class I device, cleared for Ameritek, Inc. on under FDA product code HNH (Ring, Ophthalmic (Flieringa)). FDA records list 17 510(k) clearances for Ameritek, Inc., from to . As of , FDA records show no recalls naming K863775.

Clearance record

Decision date
Received
(24 days to decision)
Product code
HNH Ring, Ophthalmic (Flieringa)
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Applicant
Ameritek, Inc. 7030 35th Ave., NE, Seattle WA
Third party review
No

Clearances, product code HNH

Trailing 12 months

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

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