510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935020Substantially Equivalent

Omni-Trac Modification

Invivo Research, Inc., Orlando FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935020 is the FDA 510(k) clearance record for OMNI-TRAC MODIFICATION, a class II device, cleared for Invivo Research, Inc. on under FDA product code MLD (Monitor, St Segment With Alarm). FDA records list 14 510(k) clearances for Invivo Research, Inc., from to . As of , FDA records show no recalls naming K935020.

Clearance record

Decision date
Received
(553 days to decision)
Product code
MLD Monitor, St Segment With Alarm
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Invivo Research, Inc. 12601 Research Pkwy., Orlando FL
510(k) summary
Statement
Third party review
No

Clearances, product code MLD

Trailing 12 months

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

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