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

Diagnostic Ultrasonic Transducer, Robotic

21 CFR 892.1570 / Radiology
FDA source (opens on fda.gov)

OQQ is the FDA product code for Diagnostic Ultrasonic Transducer, Robotic, a class II device type, regulated under 21 CFR 892.1570. FDA's definition for this code reads: "Diagnostic ultrasonic imaging or monitoring". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
OQQ
Device name
Diagnostic Ultrasonic Transducer, Robotic
FDA definition
Diagnostic ultrasonic imaging or monitoring.
Regulation
21 CFR 892.1570
Device class
Class II
Review panel
Radiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code OQQ

By decision year
1 clearance under product code OQQ with a decision year between 2010 and 2010, 2010 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code OQQ by decision year
YearClearances
20101

Applicants with the most clearances

Product code OQQ
Applicants holding the most 510(k) clearances under product code OQQ
ApplicantClearances
Shenzhen Delicate Electronics Co., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code