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
K800488Substantially Equivalent

Surgery Display System

Kent Barker & Assoc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800488 is the FDA 510(k) clearance record for SURGERY DISPLAY SYSTEM, a class II device, cleared for Kent Barker & Assoc. on under FDA product code DRQ (Amplifier And Signal Conditioner, Transducer Signal). FDA records list one 510(k) clearance for Kent Barker & Assoc. As of , FDA records show no recalls naming K800488.

Clearance record

Decision date
Received
(43 days to decision)
Product code
DRQ Amplifier And Signal Conditioner, Transducer Signal
Regulation
21 CFR 870.2060
Device class
Class II
Review panel
Cardiovascular
Applicant
Kent Barker & Assoc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DRQ

Trailing 12 months

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

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