510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K092837Substantially Equivalent

Oti-Scan 3000

Opko Instrumentation, Inc., Miami FL / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K092837 is the FDA 510(k) clearance record for OTI-SCAN 3000, a class II device, cleared for Opko Instrumentation, Inc. on under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). FDA records list one 510(k) clearance for Opko Instrumentation, Inc. As of , FDA records show no recalls naming K092837.

Clearance record

Decision date
Received
(99 days to decision)
Product code
IYO System, Imaging, Pulsed Echo, Ultrasonic
Regulation
21 CFR 892.1560
Device class
Class II
Review panel
Radiology
Applicant
Opko Instrumentation, Inc. 4400 Biscayne Blvd., Miami FL
510(k) summary
Statement
Third party review
No

Clearances, product code IYO

Trailing 12 months
8 clearances under product code IYO in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IYO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20262
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260