Terragene Bionova SCBI (BT96), Terragene Bionova Reader Incubators (IC10/20FRLCD, Mini-bio), Terragene Chemdye (CD42), Terragene Cintape (CT40)

FDA 510(k) K212193 · Plasmapp Co,., Ltd.

Substantially Equivalent

510(k) numberK212193

Submission

Device name
Terragene Bionova SCBI (BT96), Terragene Bionova Reader Incubators (IC10/20FRLCD, Mini-bio), Terragene Chemdye (CD42), Terragene Cintape (CT40)
Applicant
Plasmapp Co,., Ltd.
Daejeon, KR
Received
July 14, 2021
Decision date
October 22, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRC – Indicator, Biological Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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More from 3M Company

510(k)DeviceDecision
K231169STERLINK plus Sterilizer with STERLOAD Cassette, Tyvek Roll with CI for STERLINK…MLR · Special 05/25/2023SE
K223025Tyvek Roll with CI for STERLINK SterilizerFRG · Traditional 05/09/2023SE
K223023Terragene Bionava SCBI (BT96), Terragene Bionova Reader Incubators (IC10/20FRLCD…FRC · Traditional 05/09/2023SE
K223015STERLINK™ FPS-15s Plus sterilizer with STERPACK™ plus cassetteMLR · Traditional 05/09/2023SE
K220345STERLINK mini Sterilizer with STERLOAD mini Cassette, Tyvek Roll with CI for STERLINK…MLR · Traditional 04/14/2023SE
K212200STERLINKTM FPS-15s Plus Sterilizer with STERLOADTM CassetteMLR · Traditional 10/22/2021SE
K212198Tyvek(R) Roll with CI for STERLINKTM SterilizerFRG · Traditional 10/22/2021SE

Questions and answers

When was Terragene Bionova SCBI (BT96), Terragene Bionova Reader Incubators (IC10/20FRLCD, Mini-bio), Terragene Chemdye (CD42), Terragene Cintape (CT40) cleared by the FDA?

Terragene Bionova SCBI (BT96), Terragene Bionova Reader Incubators (IC10/20FRLCD, Mini-bio), Terragene Chemdye (CD42), Terragene Cintape (CT40) (K212193) received a 510(k) decision of Substantially Equivalent on October 22, 2021, 100 days after the submission was received.

What is the product code of K212193?

The FDA product code is FRC – Indicator, Biological Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.