510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K024080Substantially Equivalent

Secquire Cell Separator

Perfusion Partners & Assoc., Inc., Crofton MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K024080 is the FDA 510(k) clearance record for SECQUIRE CELL SEPARATOR, a class I device, cleared for Perfusion Partners & Assoc., Inc. on under FDA product code JQC (Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use). FDA records list 2 510(k) clearances for Perfusion Partners & Assoc., Inc., from to . As of , FDA records show no recalls naming K024080.

Clearance record

Decision date
Received
(204 days to decision)
Product code
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Perfusion Partners & Assoc., Inc. P.O. Box 4341, Crofton MD
510(k) summary
Statement
Third party review
No

Clearances, product code JQC

Trailing 12 months

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

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