510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780599Substantially Equivalent

Syringe, Ear & Ulcer

Abco Dealers, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780599 is the FDA 510(k) clearance record for SYRINGE, EAR & ULCER, a class I device, cleared for Abco Dealers, Inc. on under FDA product code KCP (Syringe, Ent). FDA records list 127 510(k) clearances for Abco Dealers, Inc., from to . As of , FDA records show no recalls naming K780599.

Clearance record

Decision date
Received
(9 days to decision)
Product code
KCP Syringe, Ent
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Abco Dealers, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KCP

Trailing 12 months

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

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