510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142483Substantially Equivalent

TurboSEAL Nasogastric Aspiration Tube

Turboseal, L.P., Tel Aviv, IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142483 is the FDA 510(k) clearance record for TurboSEAL Nasogastric Aspiration Tube, a class II device, cleared for Turboseal, L.P. on under FDA product code BSS (Tube, Nasogastric). FDA records list one 510(k) clearance for Turboseal, L.P. As of , FDA records show no recalls naming K142483.

Clearance record

Decision date
Received
(106 days to decision)
Product code
BSS Tube, Nasogastric
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Turboseal, L.P. 7 Haarad St., Tel Aviv, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSS

Trailing 12 months

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

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