510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K981610Substantially Equivalent

Careside Analyzer

Careside, Inc., Culver City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981610 is the FDA 510(k) clearance record for CARESIDE ANALYZER, a class I device, cleared for Careside, Inc. on under FDA product code CEO (Phosphomolybdate (Colorimetric), Inorganic Phosphorus). FDA records list 22 510(k) clearances for Careside, Inc., from to . As of , FDA records show no recalls naming K981610.

Clearance record

Decision date
Received
(56 days to decision)
Product code
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Regulation
21 CFR 862.1580
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Careside, Inc. 6100 Bristol Pkwy., Culver City CA
510(k) summary
Summary
Third party review
No

Clearances, product code CEO

Trailing 12 months

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

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