510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013412Substantially Equivalent

At Home Drug Test, Model 9069

Phamatech Inc., San Diego CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K013412 is the FDA 510(k) clearance record for AT HOME DRUG TEST, MODEL 9069, cleared for Phamatech, Inc. on under FDA product code MVO (Kit, Test, Multiple, Drugs Of Abuse, Over The Counter). FDA records list 62 510(k) clearances for Phamatech, Inc., from to . As of , FDA records show no recalls naming K013412.

Clearance record

Decision date
Received
(52 days to decision)
Product code
MVO Kit, Test, Multiple, Drugs Of Abuse, Over The Counter
Device class
Unclassified
Review panel
Unknown
Applicant
Phamatech, Inc. 9530 Padgett St., #101, San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code MVO

Trailing 12 months

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

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