510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810251Substantially Equivalent

Syringe, ENT

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

K810251 is the FDA 510(k) clearance record for SYRINGE, ENT, a class I device, cleared for Megaplast, Inc. on under FDA product code KYZ (Syringe, Irrigating (Non Dental)). FDA records list 7 510(k) clearances for Megaplast, Inc., from to . As of , FDA records show no recalls naming K810251.

Clearance record

Decision date
Received
(41 days to decision)
Product code
KYZ Syringe, Irrigating (Non Dental)
Regulation
21 CFR 880.6960
Device class
Class I
Review panel
General Hospital
Applicant
Megaplast, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KYZ

Trailing 12 months

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

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