510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913263Substantially Equivalent

Vitalmax 830 Series

Pace Tech, Inc., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913263 is the FDA 510(k) clearance record for VITALMAX 830 SERIES, a class II device, cleared for Pace Tech, Inc. on under FDA product code MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)). FDA records list 18 510(k) clearances for Pace Tech, Inc., from to . As of , FDA records show no recalls naming K913263.

Clearance record

Decision date
Received
(79 days to decision)
Product code
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Pace Tech, Inc. 510 Garden Ave. N., Clearwater FL
510(k) summary
Summary
Third party review
No

Clearances, product code MHX

Trailing 12 months
15 clearances under product code MHX in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code MHX, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20261
March 20260
April 20263
May 20262
June 20261
July 20261
August 20263
September 20261
October 20260