Ciba Corning Model 270 Co-Oximeter

FDA 510(k) K913332 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK913332

Submission

Device name
Ciba Corning Model 270 Co-Oximeter
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
July 25, 1991
Decision date
October 23, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DQA – Oximeter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2700
Specialty
Cardiovascular

Other 510(k)s with product code DQA

510(k)DeviceApplicantDecision
K252821Reusable Adult SpO2 Clip Sensor (3m) (M1196A); Reusable Adult SpO2 Clip Sensor (0.9m)…DQA · Traditional Philips Medizin Systeme Böblingen GmbH05/29/2026SE
K252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO…DQA · Traditional Shenzhen Imdk Medical Technology Co., Ltd.05/11/2026SE
K253887Nasal Alar SpO2 Sensor (989803205381); Nasal Alar SpO2 Sensor (989803205391); Nasal Alar…DQA · Traditional Philips Medizin Systeme05/01/2026SE
K260931Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)DQA · Special Unimed Medical Supplies, Inc.04/14/2026SE
K252448AViTA Pulse Oximeter (SP61)DQA · Traditional Avita Corporation02/27/2026SE
K252805YUWELL® Finger Pulse Oximeter (YX105, YX106, YX110, YX310)DQA · Traditional Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.02/17/2026SE
K253109Reusable SPO2 Sensor (BSA307-47; BSA109-50; BSA109-31O)DQA · Traditional Shenzhen Best Electronics Co., Ltd.01/07/2026SE
K251751Spo2 Sensor CSS032DDQA · Traditional Shenzhen Ykd Technology Co., Ltd.12/19/2025SE
K251696Unimed Reusable SpO2 Sensors (-48 Series and -29 Series) (U410-48); Unimed Reusable SpO2…DQA · Traditional Unimed Medical Supplies, Inc.12/01/2025SE
K251691Unimed Reusable SpO2 Sensors (-08 Series) (U403S-08); Unimed Reusable SpO2 Sensors (-08…DQA · Traditional Unimed Medical Supplies, Inc.12/01/2025SE

More from Unimed Medical Supplies, Inc.

510(k)DeviceDecision
K962559Acs Cortisol ImmunoassayJFT · Traditional 11/05/1996SE
K963251Ciba Corning ACS;180 DPD AssayJMM · Traditional 10/15/1996SE
K961807Certain HCT Level a & Level B/Cvm HCT Levels 1,2,3, & 4GLK · Traditional 07/26/1996SE
K961657Ciba Corning 400 SystemCHL · Traditional 06/25/1996SE
K962021Ciba Corning 348 SystemCHL · Traditional 06/24/1996SE
K962126Acs CKMB II ImmunoassayJHS · Traditional 06/21/1996SE
K962041Acs LH2 ImmunoassayCEP · Traditional 06/21/1996SE
K961510Acs FRT4 ImmunoassayJJX · Traditional 06/17/1996SE
K960246Liquid Cardiac Marker 1,2,3 AssayedJJT · Traditional 04/23/1996SE
K955873Acs Phenytoin AssayLGR · Traditional 03/11/1996SE

Questions and answers

When was Ciba Corning Model 270 Co-Oximeter cleared by the FDA?

Ciba Corning Model 270 Co-Oximeter (K913332) received a 510(k) decision of Substantially Equivalent on October 23, 1991, 90 days after the submission was received.

What is the product code of K913332?

The FDA product code is DQA – Oximeter, a Class II (moderate risk) device regulated under 21 CFR 870.2700.