510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791811Substantially Equivalent

Spectrum Automatic Chest Unit Model C

Spectrum X-Ray Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K791811 is the FDA 510(k) clearance record for SPECTRUM AUTOMATIC CHEST UNIT MODEL C, a class II device, cleared for Spectrum X-Ray Corp. on under FDA product code KPX (Changer, Radiographic Film/Cassette). FDA records list 9 510(k) clearances for Spectrum X-Ray Corp., from to . As of , FDA records show no recalls naming K791811.

Clearance record

Decision date
Received
(38 days to decision)
Product code
KPX Changer, Radiographic Film/Cassette
Regulation
21 CFR 892.1860
Device class
Class II
Review panel
Radiology
Applicant
Spectrum X-Ray Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KPX

Trailing 12 months

FDA records hold no clearances under product code KPX in the trailing twelve months.

FDA records show no clearances under product code KPX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260