510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K093642Substantially Equivalent

Neutrasal

Invado Pharmaceuticals, Pomona NY / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093642 is the FDA 510(k) clearance record for NEUTRASAL, cleared for Invado Pharmaceuticals on under FDA product code LFD (Saliva, Artificial). FDA records list 2 510(k) clearances for Invado Pharmaceuticals, from to . As of , FDA records show no recalls naming K093642.

Clearance record

Decision date
Received
(17 days to decision)
Product code
LFD Saliva, Artificial
Device class
Unclassified
Review panel
Unknown
Applicant
Invado Pharmaceuticals 25 Ravenna Dr., Pomona NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LFD

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