Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K032914Substantially Equivalent

Modification To:raven Bacterial Spore Strips

Raven Biological Laboratories, Inc., Omaha NE / Traditional, Substantially Equivalent

K032914 is the FDA 510(k) clearance record for MODIFICATION TO:RAVEN BACTERIAL SPORE STRIPS, a class II device, cleared for Raven Biological Laboratories, Inc. on under FDA product code FRC (Indicator, Biological Sterilization Process). FDA records list 15 510(k) clearances for Raven Biological Laboratories, Inc., from to . As of , FDA records show 2 recalls naming K032914.

Clearance record

Decision date
Received
(246 days to decision)
Product code
FRC Indicator, Biological Sterilization Process
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Raven Biological Laboratories, Inc. 8607 Park Dr., Omaha NE
510(k) summary
Statement
Third party review
No

Clearances, product code FRC

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