510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974830Substantially Equivalent

Ultra Bili Light

Physician Engineered Products, Inc., Park Rapids MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974830 is the FDA 510(k) clearance record for ULTRA BILI LIGHT, a class II device, cleared for Physician Engineered Products, Inc. on under FDA product code LBI (Unit, Neonatal Phototherapy). FDA records list 8 510(k) clearances for Physician Engineered Products, Inc., from to . As of , FDA records show no recalls naming K974830.

Clearance record

Decision date
Received
(147 days to decision)
Product code
LBI Unit, Neonatal Phototherapy
Regulation
21 CFR 880.5700
Device class
Class II
Review panel
General Hospital
Applicant
Physician Engineered Products, Inc. 420 W. Second St., Park Rapids MN
510(k) summary
Statement
Third party review
No

Clearances, product code LBI

Trailing 12 months
1 clearance under product code LBI in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LBI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260