510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K042484Substantially Equivalent

Nai Tech Products Medical Digital Recorder

Nai Technology Products, Upland CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K042484 is the FDA 510(k) clearance record for NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER, a class II device, cleared for Nai Technology Products on under FDA product code LMA (Digitizer, Image, Radiological). FDA records list one 510(k) clearance for Nai Technology Products. As of , FDA records show no recalls naming K042484.

Clearance record

Decision date
Received
(37 days to decision)
Product code
LMA Digitizer, Image, Radiological
Regulation
21 CFR 892.2030
Device class
Class II
Review panel
Radiology
Applicant
Nai Technology Products 1342-D N. Benson Ave., Upland CA
510(k) summary
Statement
Third party review
No

Clearances, product code LMA

Trailing 12 months

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

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