510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884722Substantially Equivalent

Lumineb I

Lumiscope Co., Inc., Edison NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884722 is the FDA 510(k) clearance record for LUMINEB I, a class II device, cleared for Lumiscope Co., Inc. on under FDA product code BTI (Compressor, Air, Portable). FDA records list 13 510(k) clearances for Lumiscope Co., Inc., from to . As of , FDA records show no recalls naming K884722.

Clearance record

Decision date
Received
(85 days to decision)
Product code
BTI Compressor, Air, Portable
Regulation
21 CFR 868.6250
Device class
Class II
Review panel
Anesthesiology
Applicant
Lumiscope Co., Inc. 400 Raritan Center Pkwy., Edison NJ
Third party review
No

Clearances, product code BTI

Trailing 12 months

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

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