510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980896Substantially Equivalent

Quickcard Pro Hcg Test, Model 9008

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

K980896 is the FDA 510(k) clearance record for QUICKCARD PRO HCG TEST, MODEL 9008, a class II device, cleared for Phamatech on under FDA product code JHI (Visual, Pregnancy Hcg, Prescription Use). FDA records list 62 510(k) clearances for Phamatech, from to . As of , FDA records show no recalls naming K980896.

Clearance record

Decision date
Received
(24 days to decision)
Product code
JHI Visual, Pregnancy Hcg, Prescription Use
Regulation
21 CFR 862.1155
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Phamatech 9265 Activity Rd., #112-113, San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code JHI

Trailing 12 months
1 clearance under product code JHI in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JHI, 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 20261
October 20260