Pulse Oximeter, Models PC-66A; PC-66B; PC-66C;PC-60B1; PC-60B5; PC-60D; PC-60D2; PC-60E; PC-60N; POD-1; POD-2; POD-3; PC-68A; PC-68B; PC-68C; POD- 1W; and POD-60NW-1

FDA 510(k) K150093 · Shenzhen Creative Industry Co., Ltd.

Substantially Equivalent

510(k) numberK150093

Submission

Device name
Pulse Oximeter, Models PC-66A; PC-66B; PC-66C;PC-60B1; PC-60B5; PC-60D; PC-60D2; PC-60E; PC-60N; POD-1; POD-2; POD-3; PC-68A; PC-68B; PC-68C; POD- 1W; and POD-60NW-1
Applicant
Shenzhen Creative Industry Co., Ltd.
Shenzhen City, CN
Received
January 16, 2015
Decision date
June 3, 2015
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary 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

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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
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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

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K172792Handheld Pulse Oximeter, Model SP-20DQA · Traditional 11/13/2018SE
K170047All-in-One Health Monitor, PC-303MWI · Traditional 09/09/2017SE
K123711Patient MonitorMWI · Traditional 10/01/2013SE
K120502PC-60NW Fingertip OximeterDQA · Abbreviated 12/07/2012SE
K093016Vital Signs MonitorDQA · Traditional 03/30/2010SE
K082055Model PC-860 Fetal DopplerKNG · Traditional 02/06/2009SE
K073152PC-180 / Prince 180 Easy ECG MonitorDSH · Traditional 01/10/2008SE
K063641PC-60, Non-Invasivepulse OximeterDQA · Traditional 07/13/2007SE

Questions and answers

When was Pulse Oximeter, Models PC-66A; PC-66B; PC-66C;PC-60B1; PC-60B5; PC-60D; PC-60D2; PC-60E; PC-60N; POD-1; POD-2; POD-3; PC-68A; PC-68B; PC-68C; POD- 1W; and POD-60NW-1 cleared by the FDA?

Pulse Oximeter, Models PC-66A; PC-66B; PC-66C;PC-60B1; PC-60B5; PC-60D; PC-60D2; PC-60E; PC-60N; POD-1; POD-2; POD-3; PC-68A; PC-68B; PC-68C; POD- 1W; and POD-60NW-1 (K150093) received a 510(k) decision of Substantially Equivalent on June 3, 2015, 138 days after the submission was received.

What is the product code of K150093?

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