510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K935691Substantially Equivalent

Model Gp-252 General Purpose Coil

Diagnostic Instrument Corp., Aurora OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935691 is the FDA 510(k) clearance record for MODEL GP-252 GENERAL PURPOSE COIL, a class II device, cleared for Diagnostic Instrument Corp. on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 2 510(k) clearances for Diagnostic Instrument Corp., from to . As of , FDA records show no recalls naming K935691.

Clearance record

Decision date
Received
(245 days to decision)
Product code
LNH System, Nuclear Magnetic Resonance Imaging
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Diagnostic Instrument Corp. 201 Belcourt Ln., Aurora OH
510(k) summary
Statement
Third party review
No

Clearances, product code LNH

Trailing 12 months
26 clearances under product code LNH in the twelve months to October 2026, March 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code LNH, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20266
April 20261
May 20261
June 20260
July 20262
August 20263
September 20263
October 20261