510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842517Substantially Equivalent

Unilet Lancet

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

K842517 is the FDA 510(k) clearance record for UNILET LANCET, a class I device, cleared for Ulster Scientific, Inc. on under FDA product code FML (Chair, Blood Donor). FDA records list 20 510(k) clearances for Ulster Scientific, Inc., from to . As of , FDA records show no recalls naming K842517.

Clearance record

Decision date
Received
(72 days to decision)
Product code
FML Chair, Blood Donor
Regulation
21 CFR 880.6140
Device class
Class I
Review panel
General Hospital
Applicant
Ulster Scientific, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FML

Trailing 12 months

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

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