510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K864467Substantially Equivalent

Henson - Hamblin Cfs 2000 Central Field Screen

Keeler Instruments, Inc., Broomall PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864467 is the FDA 510(k) clearance record for HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN, a class I device, cleared for Keeler Instruments, Inc. on under FDA product code HOO (Perimeter, Ac-Powered). FDA records list 60 510(k) clearances for Keeler Instruments, Inc., from to . As of , FDA records show no recalls naming K864467.

Clearance record

Decision date
Received
(33 days to decision)
Product code
HOO Perimeter, Ac-Powered
Regulation
21 CFR 886.1605
Device class
Class I
Review panel
Ophthalmic
Applicant
Keeler Instruments, Inc. 456 Pkwy., Broomall PA
Third party review
No

Clearances, product code HOO

Trailing 12 months

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

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