510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K860282Substantially Equivalent

Rpmi 1640 W/glutamine W/hepes

Newport Biosystems, Inc., Santa Ana CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860282 is the FDA 510(k) clearance record for RPMI 1640 W/GLUTAMINE W/HEPES, a class I device, cleared for Newport Biosystems, Inc. on under FDA product code KIT (Media And Components, Synthetic Cell And Tissue Culture). FDA records list 4 510(k) clearances for Newport Biosystems, Inc., from to . As of , FDA records show no recalls naming K860282.

Clearance record

Decision date
Received
(8 days to decision)
Product code
KIT Media And Components, Synthetic Cell And Tissue Culture
Regulation
21 CFR 864.2220
Device class
Class I
Review panel
Hematology
Applicant
Newport Biosystems, Inc. Rod Roberts, Santa Ana CA
Third party review
No

Clearances, product code KIT

Trailing 12 months

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

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