510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K053625Substantially Equivalent

Nasalguard

Trutek Corp, Somerville NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K053625 is the FDA 510(k) clearance record for NASALGUARD, a class II device, cleared for Trutek Corp on under FDA product code NUP (Cream, Nasal, Topical, Mechanical Allergen Particle Barrier). FDA's definition for product code NUP reads: "THE DEVICE IS INTENDED TO PROMOTE ALLEVIATION OF MILD ALLERGIC SYMPTOMS TRIGGERED BY THE INHALATION OF VARIOUS ALLERGENS". FDA records list 2 510(k) clearances for Trutek Corp, from to . As of , FDA records show no recalls naming K053625.

Clearance record

Decision date
Received
(56 days to decision)
Product code
NUP Cream, Nasal, Topical, Mechanical Allergen Particle Barrier
Regulation
21 CFR 880.5045
Device class
Class II
Review panel
General Hospital
Applicant
Trutek Corp 80 W. End Ave., Somerville NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NUP

Trailing 12 months

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

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