510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K200722Substantially Equivalent

PCA-C1 series Patient Cable

QT Medical, Inc, Diamond Bar CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K200722 is the FDA 510(k) clearance record for PCA-C1 series Patient Cable, a class II device, cleared for QT Medical, Inc. on under FDA product code DSA (Cable, Transducer And Electrode, Patient, (Including Connector)). FDA records list 4 510(k) clearances for QT Medical, Inc., from to . As of , FDA records show no recalls naming K200722.

Clearance record

Decision date
Received
(441 days to decision)
Product code
DSA Cable, Transducer And Electrode, Patient, (Including Connector)
Regulation
21 CFR 870.2900
Device class
Class II
Review panel
Cardiovascular
Applicant
QT Medical, Inc. 1360 Valley Vista Dr., Diamond Bar CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DSA

Trailing 12 months
2 clearances under product code DSA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260