510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K873834Substantially Equivalent

Inet Model Biovision

Inet Corp., Newark CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873834 is the FDA 510(k) clearance record for INET MODEL BIOVISION, a class II device, cleared for Inet Corp. on under FDA product code HCC (Device, Biofeedback). FDA records list one 510(k) clearance for Inet Corp. As of , FDA records show no recalls naming K873834.

Clearance record

Decision date
Received
(185 days to decision)
Product code
HCC Device, Biofeedback
Regulation
21 CFR 882.5050
Device class
Class II
Review panel
Neurology
Applicant
Inet Corp. 8450 Central Ave., Newark CA
Third party review
No

Clearances, product code HCC

Trailing 12 months

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

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