510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K883609Substantially Equivalent

Acces. Package for Use W/cardiogen-82 Generator

Squibb Diagnostics, New Brunswick NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883609 is the FDA 510(k) clearance record for ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR, a class II device, cleared for Squibb Diagnostics on under FDA product code FRN (Pump, Infusion). FDA records list 3 510(k) clearances for Squibb Diagnostics, from to . As of , FDA records show no recalls naming K883609.

Clearance record

Decision date
Received
(235 days to decision)
Product code
FRN Pump, Infusion
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Squibb Diagnostics P.O. Box 191, New Brunswick NJ
Third party review
No

Clearances, product code FRN

Trailing 12 months
2 clearances under product code FRN in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FRN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260