510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781218Substantially Equivalent

Anemometer, Nasal, Exeter

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

K781218 is the FDA 510(k) clearance record for ANEMOMETER, NASAL, EXETER, cleared for Medika Corp. on under FDA product code ETL. FDA records list one 510(k) clearance for Medika Corp. As of , FDA records show no recalls naming K781218.

Clearance record

Decision date
Received
(10 days to decision)
Product code
ETL
Review panel
Unknown
Applicant
Medika Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ETL

Trailing 12 months

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

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