Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K892347Substantially Equivalent

Magnilink System 101

Coburn Optical Ind., Inc., Tulsa OK / Traditional, Substantially Equivalent

K892347 is the FDA 510(k) clearance record for MAGNILINK SYSTEM 101, a class I device, cleared for Coburn Optical Ind., Inc. on under FDA product code HJG (System, Reading, Television, Closed-Circuit). FDA records list 14 510(k) clearances for Coburn Optical Ind., Inc., from to . As of , FDA records show no recalls naming K892347.

Clearance record

Decision date
Received
(51 days to decision)
Product code
HJG System, Reading, Television, Closed-Circuit
Regulation
21 CFR 886.5820
Device class
Class I
Review panel
Ophthalmic
Applicant
Coburn Optical Ind., Inc. 4606 S. Garnett Rd., Tulsa OK
Third party review
No

Clearances, product code HJG

Trailing 12 months

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

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