510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K982491Substantially Equivalent

Sangui Biotech, Inc. Calcitonin Elisa Kit

Sangui Biotech, Inc., Santa Ana CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K982491 is the FDA 510(k) clearance record for SANGUI BIOTECH, INC. CALCITONIN ELISA KIT, a class II device, cleared for Sangui Biotech, Inc. on under FDA product code JKR (Radioimmunoassay, Calcitonin). FDA records list 5 510(k) clearances for Sangui Biotech, Inc., from to . As of , FDA records show one recall naming K982491.

Clearance record

Decision date
Received
(48 days to decision)
Product code
JKR Radioimmunoassay, Calcitonin
Regulation
21 CFR 862.1140
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sangui Biotech, Inc. 1508 Brookhollow Dr., #354, Santa Ana CA
510(k) summary
Summary
Third party review
No

Clearances, product code JKR

Trailing 12 months
1 clearance under product code JKR in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JKR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260