Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K780488Substantially Equivalent

Instrument and Accessory Kit

American Hospital Supply, Mchenry IL / Traditional, Substantially Equivalent

K780488 is the FDA 510(k) clearance record for INSTRUMENT AND ACCESSORY KIT, a class I device, cleared for American Hospital Supply Corp. on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 56 510(k) clearances for American Hospital Supply Corp., from to . As of , FDA records show no recalls naming K780488.

Clearance record

Decision date
Received
(16 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
American Hospital Supply Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

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