510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K891604Substantially Equivalent

The Cen-Slide(tm) Centrifuge Tube

Davstar California, Inc., Lawndale CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891604 is the FDA 510(k) clearance record for THE CEN-SLIDE(TM) CENTRIFUGE TUBE, a class I device, cleared for Davstar California, Inc. on under FDA product code KEW (Slides, Microscope). FDA records list one 510(k) clearance for Davstar California, Inc. As of , FDA records show no recalls naming K891604.

Clearance record

Decision date
Received
(88 days to decision)
Product code
KEW Slides, Microscope
Regulation
21 CFR 864.3010
Device class
Class I
Review panel
Pathology
Applicant
Davstar California, Inc. 15223 Grevillea Ave., Lawndale CA
Third party review
No

Clearances, product code KEW

Trailing 12 months

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

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