510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821337Substantially Equivalent

Shigella I.d.

Analytical Products, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821337 is the FDA 510(k) clearance record for SHIGELLA I.D., a class II device, cleared for Analytical Products, Inc. on under FDA product code GNB (Antisera, All Types, Shigella Spp.). FDA records list 57 510(k) clearances for Analytical Products, Inc., from to . As of , FDA records show no recalls naming K821337.

Clearance record

Decision date
Received
(23 days to decision)
Product code
GNB Antisera, All Types, Shigella Spp.
Regulation
21 CFR 866.3660
Device class
Class II
Review panel
Microbiology
Applicant
Analytical Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GNB

Trailing 12 months

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

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