510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K850371Substantially Equivalent

Intiwash Manual Microplate Washer

Inti Corp., San Rafael CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850371 is the FDA 510(k) clearance record for INTIWASH MANUAL MICROPLATE WASHER, a class I device, cleared for Inti Corp. on under FDA product code JTC (Device, Microtiter Diluting/Dispensing). FDA records list one 510(k) clearance for Inti Corp. As of , FDA records show no recalls naming K850371.

Clearance record

Decision date
Received
(39 days to decision)
Product code
JTC Device, Microtiter Diluting/Dispensing
Regulation
21 CFR 866.2500
Device class
Class I
Review panel
Microbiology
Applicant
Inti Corp. P.O. Box 6145, San Rafael CA
Third party review
No

Clearances, product code JTC

Trailing 12 months

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

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