510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901450Substantially Equivalent

Modified Label for Embria-Ck, Quick-Mb/micromi-Mb

Intl. Immunoassay Laboratories, Inc., Santa Clara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901450 is the FDA 510(k) clearance record for MODIFIED LABEL FOR EMBRIA-CK, QUICK-MB/MICROMI-MB, a class II device, cleared for Intl. Immunoassay Laboratories, Inc. on under FDA product code JHT (Chromatographic Separation, Cpk Isoenzymes). FDA records list 27 510(k) clearances for Intl. Immunoassay Laboratories, Inc., from to . As of , FDA records show no recalls naming K901450.

Clearance record

Decision date
Received
(48 days to decision)
Product code
JHT Chromatographic Separation, Cpk Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Intl. Immunoassay Laboratories, Inc. 1900 Wyatt Dr., #11, Santa Clara CA
Third party review
No

Clearances, product code JHT

Trailing 12 months

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

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