510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K900921Substantially Equivalent

Hycor Accupinch Phencyclidine Test

Hycor Biomedical, Garden Grove CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900921 is the FDA 510(k) clearance record for HYCOR ACCUPINCH PHENCYCLIDINE TEST, cleared for Hycor Biomedical, Inc. on under FDA product code LCM (Enzyme Immunoassay, Phencyclidine). FDA records list 66 510(k) clearances for Hycor Biomedical, Inc., from to . As of , FDA records show no recalls naming K900921.

Clearance record

Decision date
Received
(58 days to decision)
Product code
LCM Enzyme Immunoassay, Phencyclidine
Device class
Unclassified
Review panel
Unknown
Applicant
Hycor Biomedical, Inc. 7272 Chapman Ave., Garden Grove CA
Third party review
No

Clearances, product code LCM

Trailing 12 months

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

FDA records show no clearances under product code LCM in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LCM, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260