510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000610Substantially Equivalent

Resolution Cholesterol Monitor

Lifestream Technologies, Inc., Post Falls ID / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000610 is the FDA 510(k) clearance record for RESOLUTION CHOLESTEROL MONITOR, a class I device, cleared for Lifestream Technologies, Inc. on under FDA product code CHH (Enzymatic Esterase--Oxidase, Cholesterol). FDA records list 3 510(k) clearances for Lifestream Technologies, Inc., from to . As of , FDA records show no recalls naming K000610.

Clearance record

Decision date
Received
(149 days to decision)
Product code
CHH Enzymatic Esterase--Oxidase, Cholesterol
Regulation
21 CFR 862.1175
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Lifestream Technologies, Inc. 51o Clearwater Loop, Suite 101, Post Falls ID
510(k) summary
Summary
Third party review
No

Clearances, product code CHH

Trailing 12 months
1 clearance under product code CHH in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CHH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260