510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K863660Substantially Equivalent

Emds Uric Acid (Urc a) Testpack, Item #67664/95

Em Diagnostic Systems, Inc., Gibbstown NJ / Traditional, Substantially Equivalent

K863660 is the FDA 510(k) clearance record for EMDS URIC ACID (URC A) TESTPACK, ITEM #67664/95, a class I device, cleared for Em Diagnostic Systems, Inc. on under FDA product code CDO (Acid, Uric, Uricase (U.V.)). FDA records list 288 510(k) clearances for Em Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K863660.

Clearance record

Decision date
Received
(41 days to decision)
Product code
CDO Acid, Uric, Uricase (U.V.)
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Em Diagnostic Systems, Inc. 480 Democrat Rd., Gibbstown NJ
Third party review
No

Clearances, product code CDO

Trailing 12 months

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

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