510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932139Substantially Equivalent

Lighted Intubation Stylet W/replaceable Shaft

Apyx Medical Corporation, St. Petersburg FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932139 is the FDA 510(k) clearance record for LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT, a class II device, cleared for Aaron Medical Industries on under FDA product code FSQ (Light, Surgical, Instrument). FDA records list 75 510(k) clearances for Apyx Medical Corporation, from to . As of , FDA records show no recalls naming K932139.

Clearance record

Decision date
Received
(87 days to decision)
Product code
FSQ Light, Surgical, Instrument
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Aaron Medical Industries 7100 30th Ave. N, St. Petersburg FL
510(k) summary
Statement
Third party review
No

Clearances, product code FSQ

Trailing 12 months

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

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