510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800554Substantially Equivalent

Multi-Format Sfd Model 1720

Philips North America LLC, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800554 is the FDA 510(k) clearance record for MULTI-FORMAT SFD MODEL 1720, a class II device, cleared for Philips Medical Systems (Cleveland), Inc. on under FDA product code IXL (Device, Spot-Film). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show no recalls naming K800554.

Clearance record

Decision date
Received
(29 days to decision)
Product code
IXL Device, Spot-Film
Regulation
21 CFR 892.1670
Device class
Class II
Review panel
Radiology
Applicant
Philips Medical Systems (Cleveland), Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IXL

Trailing 12 months

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

FDA records show no clearances under product code IXL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IXL, 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