510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940074Substantially Equivalent

Y-Type Blood Administration Set

Puritas Health Care, Inc., New Milford CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940074 is the FDA 510(k) clearance record for Y-TYPE BLOOD ADMINISTRATION SET, a class II device, cleared for Puritas Health Care, Inc. on under FDA product code BRZ (Set, Blood Transfusion). FDA records list 24 510(k) clearances for Puritas Health Care, Inc., from to . As of , FDA records show no recalls naming K940074.

Clearance record

Decision date
Received
(105 days to decision)
Product code
BRZ Set, Blood Transfusion
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Puritas Health Care, Inc. 219 Kent Rd.,, New Milford CT
510(k) summary
Statement
Third party review
No

Clearances, product code BRZ

Trailing 12 months

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

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