510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830705Substantially Equivalent

Mini Lancet-Blood Lancet

Pharmaquest Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830705 is the FDA 510(k) clearance record for MINI LANCET-BLOOD LANCET, a class I device, cleared for Pharmaquest Corp. on under FDA product code FMA (Depressor, Tongue, Non-Surgical). FDA records list 14 510(k) clearances for Pharmaquest Corp., from to . As of , FDA records show no recalls naming K830705.

Clearance record

Decision date
Received
(32 days to decision)
Product code
FMA Depressor, Tongue, Non-Surgical
Regulation
21 CFR 880.6230
Device class
Class I
Review panel
General Hospital
Applicant
Pharmaquest Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FMA

Trailing 12 months

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

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