510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832088Substantially Equivalent

Ames Tda Netilmicin Test & Serum

Miles Laboratories, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832088 is the FDA 510(k) clearance record for AMES TDA NETILMICIN TEST & SERUM, a class II device, cleared for Miles Laboratories, Inc. on under FDA product code LCE (Radioimmunoassay, Netilmicin (I-125)). FDA records list 158 510(k) clearances for Miles Laboratories, Inc., from to . As of , FDA records show no recalls naming K832088.

Clearance record

Decision date
Received
(122 days to decision)
Product code
LCE Radioimmunoassay, Netilmicin (I-125)
Regulation
21 CFR 862.3450
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Miles Laboratories, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code LCE

Trailing 12 months

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

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