510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K140651Substantially Equivalent

Celesteion, Pca-9000A/2

Toshibamedical Systems Corporation, Tustin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140651 is the FDA 510(k) clearance record for CELESTEION, PCA-9000A/2, a class II device, cleared for Toshibamedical Systems Corporation on under FDA product code KPS (System, Tomography, Computed, Emission). FDA records list 80 510(k) clearances for Toshibamedical Systems Corporation, from to . As of , FDA records show 2 recalls naming K140651.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KPS System, Tomography, Computed, Emission
Regulation
21 CFR 892.1200
Device class
Class II
Review panel
Radiology
Applicant
Toshibamedical Systems Corporation 2441 Michelle Dr., Tustin 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