510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792696Substantially Equivalent

Micropitette

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

K792696 is the FDA 510(k) clearance record for MICROPITETTE, a class I device, cleared for Meridian Diagnostics, Inc. on under FDA product code JRC (Micro Pipette). FDA records list 92 510(k) clearances for Meridian Diagnostics, Inc., from to . As of , FDA records show no recalls naming K792696.

Clearance record

Decision date
Received
(36 days to decision)
Product code
JRC Micro Pipette
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Meridian Diagnostics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JRC

Trailing 12 months

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

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