510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252228Substantially Equivalent

Seaman Pro/Seaman

Checkcells, Inc., Santa Monica CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252228 is the FDA 510(k) clearance record for Seaman Pro/Seaman, a class II device, cleared for Checkcells, Inc. on under FDA product code POV (Semen Analysis Device). FDA's definition for product code POV reads: "Device used to evaluate one or more human semen parameters including semen volume, sperm concentration, total sperm number, sperm motility, sperm morphology, sperm vitality, white blood cell concentration, and pH". FDA records list one 510(k) clearance for Checkcells, Inc. As of , FDA records show no recalls naming K252228.

Clearance record

Decision date
Received
(267 days to decision)
Product code
POV Semen Analysis Device
Regulation
21 CFR 864.5220
Device class
Class II
Review panel
Hematology
Applicant
Checkcells, Inc. 1725 Ocean Front Walk, Santa Monica CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code POV

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