510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K111060Substantially Equivalent

Mrgfus Pelvic Pa Coil Model 1.0

Insightech, Ltd., Tirat Carmel, IL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111060 is the FDA 510(k) clearance record for MRGFUS PELVIC PA COIL MODEL 1.0, a class II device, cleared for Insightech, Ltd. on under FDA product code MOS (Coil, Magnetic Resonance, Specialty). FDA records list one 510(k) clearance for Insightech, Ltd. As of , FDA records show no recalls naming K111060.

Clearance record

Decision date
Received
(144 days to decision)
Product code
MOS Coil, Magnetic Resonance, Specialty
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Insightech, Ltd. 5 Nahum Heth St., Tirat Carmel, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MOS

Trailing 12 months
9 clearances under product code MOS 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 MOS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20261
March 20261
April 20263
May 20260
June 20260
July 20262
August 20260
September 20260
October 20260