510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873137Substantially Equivalent

In Vitro 2.5X Roller Bottle

In Vitro Scientific Products, Oak View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873137 is the FDA 510(k) clearance record for IN VITRO 2.5X ROLLER BOTTLE, a class I device, cleared for In Vitro Scientific Products on under FDA product code KJC (Bottle, Roller, Tissue Culture). FDA records list one 510(k) clearance for In Vitro Scientific Products. As of , FDA records show no recalls naming K873137.

Clearance record

Decision date
Received
(14 days to decision)
Product code
KJC Bottle, Roller, Tissue Culture
Regulation
21 CFR 864.2240
Device class
Class I
Review panel
Hematology
Applicant
In Vitro Scientific Products 2350 Valley Meadow Dr., Oak View CA
Third party review
No

Clearances, product code KJC

Trailing 12 months

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

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