510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K973176Unknown

Seizure Emergency Equipment Kit; Seizure Kit

Lotus Technologies, Austin TX / Traditional, Unknown
FDA source (opens on fda.gov)

K973176 is the FDA 510(k) clearance record for SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT, cleared for Lotus Technologies on under FDA product code KGA. FDA records list one 510(k) clearance for Lotus Technologies. As of , FDA records show no recalls naming K973176.

Clearance record

Decision date
Received
(88 days to decision)
Product code
KGA
Review panel
Unknown
Applicant
Lotus Technologies 1215 Red River St., Austin TX
510(k) summary
Statement
Third party review
No

Clearances, product code KGA

Trailing 12 months

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

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