510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993317Substantially Equivalent

Acon Hcg One Step Pregnancy Test Device (Urine)

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

K993317 is the FDA 510(k) clearance record for ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE), a class II device, cleared for ACON Laboratories, Inc. on under FDA product code JHI (Visual, Pregnancy Hcg, Prescription Use). FDA records list 93 510(k) clearances for ACON Laboratories, Inc., from to . As of , FDA records show one recall naming K993317.

Clearance record

Decision date
Received
(58 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
ACON Laboratories, Inc. 11175 Flintkote Ave., #F, 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