510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912880Substantially Equivalent

Vitalmax 510/520

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

K912880 is the FDA 510(k) clearance record for VITALMAX 510/520, a class II device, cleared for Pace Tech, Inc. on under FDA product code DQA (Oximeter). FDA records list 18 510(k) clearances for Pace Tech, Inc., from to . As of , FDA records show no recalls naming K912880.

Clearance record

Decision date
Received
(136 days to decision)
Product code
DQA Oximeter
Regulation
21 CFR 870.2700
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 DQA

Trailing 12 months
12 clearances under product code DQA in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQA, trailing twelve months
MonthClearances
November 20252
December 20253
January 20261
February 20262
March 20260
April 20261
May 20263
June 20260
July 20260
August 20260
September 20260
October 20260