510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864436Substantially Equivalent

Stavip 3000

Roseburg SA, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864436 is the FDA 510(k) clearance record for STAVIP 3000, a class I device, cleared for Roseburg SA on under FDA product code JJN (Apparatus, Electrophoresis, For Clinical Use). FDA records list 24 510(k) clearances for Roseburg SA, from to . As of , FDA records show no recalls naming K864436.

Clearance record

Decision date
Received
(124 days to decision)
Product code
JJN Apparatus, Electrophoresis, For Clinical Use
Regulation
21 CFR 862.2485
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Roseburg SA Suite 120 Canal Sq., Washington DC
Third party review
No

Clearances, product code JJN

Trailing 12 months

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

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