510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K021423Substantially Equivalent

Instant-View Fecal Occult Blood Rapid Test

Alfa Scientific Designs, Inc., Poway CA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K021423 is the FDA 510(k) clearance record for INSTANT-VIEW FECAL OCCULT BLOOD RAPID TEST, a class II device, cleared for Alfa Scientific Designs, Inc. on under FDA product code KHE (Reagent, Occult Blood). FDA records list 43 510(k) clearances for Alfa Scientific Designs, Inc., from to . As of , FDA records show no recalls naming K021423.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KHE Reagent, Occult Blood
Regulation
21 CFR 864.6550
Device class
Class II
Review panel
Hematology
Applicant
Alfa Scientific Designs, Inc. 12330 Stowe Dr., Poway CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KHE

Trailing 12 months

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

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