Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K941983Substantially Equivalent

Sealite Sciences Inc.

Sealite Sciences, Inc., Bogart GA / Traditional, Substantially Equivalent

K941983 is the FDA 510(k) clearance record for SEALITE SCIENCES INC., a class II device, cleared for Sealite Sciences, Inc. on under FDA product code DHA (System, Test, Human Chorionic Gonadotropin). FDA records list 11 510(k) clearances for Sealite Sciences, Inc., from to . As of , FDA records show no recalls naming K941983.

Clearance record

Decision date
Received
(115 days to decision)
Product code
DHA System, Test, Human Chorionic Gonadotropin
Regulation
21 CFR 862.1155
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sealite Sciences, Inc. 187 Ben Burton Cir., Bogart GA
510(k) summary
Summary
Third party review
No

Clearances, product code DHA

Trailing 12 months

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

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