510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930141Substantially Equivalent

Synelisa Sm Abs/rnp-Sm ABS

Elias U.S.A., Inc., Osceola WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930141 is the FDA 510(k) clearance record for SYNELISA SM ABS/RNP-SM ABS, a class II device, cleared for Elias U.S.A., Inc. on under FDA product code LKP (Anti-Sm Antibody, Antigen And Control). FDA records list 54 510(k) clearances for Elias U.S.A., Inc., from to . As of , FDA records show no recalls naming K930141.

Clearance record

Decision date
Received
(119 days to decision)
Product code
LKP Anti-Sm Antibody, Antigen And Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Elias U.S.A., Inc. 373 280th St., Osceola WI
510(k) summary
Statement
Third party review
No

Clearances, product code LKP

Trailing 12 months

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

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