510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K991067Substantially Equivalent

Modification of: Davidstrip Hcg

Simex Medical, Inc., Tukwila WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K991067 is the FDA 510(k) clearance record for MODIFICATION OF: DAVIDSTRIP HCG, a class II device, cleared for Simex Medical, Inc. on under FDA product code JHI (Visual, Pregnancy Hcg, Prescription Use). FDA records list one 510(k) clearance for Simex Medical, Inc. As of , FDA records show no recalls naming K991067.

Clearance record

Decision date
Received
(28 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
Simex Medical, Inc. 560 Industry Dr., Tukwila WA
510(k) summary
Statement
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