510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K971919Substantially Equivalent

Ezchek/hba Blood Collection Kit

Flexsite Diagnostics, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K971919 is the FDA 510(k) clearance record for EZCHEK/HBA BLOOD COLLECTION KIT, a class II device, cleared for Flexsite Diagnostics, Inc. on under FDA product code LCP (Assay, Glycosylated Hemoglobin). FDA records list 2 510(k) clearances for Flexsite Diagnostics, Inc., from to . As of , FDA records show no recalls naming K971919.

Clearance record

Decision date
Received
(105 days to decision)
Product code
LCP Assay, Glycosylated Hemoglobin
Regulation
21 CFR 864.7470
Device class
Class II
Review panel
Hematology
Applicant
Flexsite Diagnostics, Inc. 1900 K St. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code LCP

Trailing 12 months

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

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