510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K882252Substantially Equivalent

Phase II Lh Kit

Vitek Systems, Inc., Rockland MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882252 is the FDA 510(k) clearance record for PHASE II LH KIT, a class I device, cleared for Vitek Systems, Inc. on under FDA product code CEP (Radioimmunoassay, Luteinizing Hormone). FDA records list 39 510(k) clearances for Vitek Systems, Inc., from to . As of , FDA records show no recalls naming K882252.

Clearance record

Decision date
Received
(65 days to decision)
Product code
CEP Radioimmunoassay, Luteinizing Hormone
Regulation
21 CFR 862.1485
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Vitek Systems, Inc. 1022 Hingham St., Rockland MA
Third party review
No

Clearances, product code CEP

Trailing 12 months

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

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