510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792013Substantially Equivalent

Lancer L-Ina Human Reference Serum

Sherwood Medical Industries, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792013 is the FDA 510(k) clearance record for LANCER L-INA HUMAN REFERENCE SERUM, a class II device, cleared for Sherwood Medical Industries on under FDA product code JIX (Calibrator, Multi-Analyte Mixture). FDA records list 62 510(k) clearances for Sherwood Medical Industries, from to . As of , FDA records show no recalls naming K792013.

Clearance record

Decision date
Received
(39 days to decision)
Product code
JIX Calibrator, Multi-Analyte Mixture
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sherwood Medical Industries 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JIX

Trailing 12 months

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

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