FDA 510(k), K200240, Turbett Instrument Pod

510(K) Number: K200240
Device Name: Turbett Instrument Pod
Manufacturer: Turbett Surgical Inc.
Device Classification Name: wrap, sterilization
Regulation Number: 880.6850
Classification Product Code: FRG
Date Received: 01/31/2020
Decision Date: 04/30/2020
Regulation Medical Specialty: General Hospital

134 pages (232 of 366 original pages are fully redacted)