510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K180077Substantially Equivalent

NeuroQ 3.8

Syntermed, Inc., Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K180077 is the FDA 510(k) clearance record for NeuroQ 3.8, a class II device, cleared for Syntermed on under FDA product code KPS (System, Tomography, Computed, Emission). FDA records list 14 510(k) clearances for Syntermed, from to . As of , FDA records show no recalls naming K180077.

Clearance record

Decision date
Received
(218 days to decision)
Product code
KPS System, Tomography, Computed, Emission
Regulation
21 CFR 892.1200
Device class
Class II
Review panel
Radiology
Applicant
Syntermed 245 S. Owens Dr., Anaheim CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KPS

Trailing 12 months
9 clearances under product code KPS in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KPS, trailing twelve months
MonthClearances
November 20251
December 20252
January 20261
February 20261
March 20260
April 20261
May 20261
June 20260
July 20261
August 20260
September 20261
October 20260