Analyzer, Oxygen, Model OM-92
FDA 510(k) K771028 · Cavitron Corp.
510(k) numberK771028
Submission
- Device name
- Analyzer, Oxygen, Model OM-92
- Applicant
- Cavitron Corp.
Mchenry, IL, US - Received
- June 9, 1977
- Decision date
- July 5, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CCL – Analyzer, Gas, Oxygen, Gaseous-Phase
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.1720
- Specialty
- Anesthesiology
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|---|---|---|---|
| K261389 | PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)CCL · Traditional | Salter Labs | 07/30/2026SE |
| K251245 | OxyMinder Pro (10310)CCL · Traditional | Bio-Med Device, Inc. | 08/11/2025SE |
| K250002 | Smart Check O2 (MA0236)CCL · Traditional | Life Spark Medical, LLC | 04/24/2025SE |
| K221734 | Maxtec MaxO2 ME+pCCL · Traditional | Maxtec, LLC | 04/01/2023SE |
| K213933 | Percent Oxygen SensorsCCL · Traditional | Careox, LLC | 08/19/2022SE |
| K213948 | OxyMinderCCL · Traditional | Bio-Med Devices, Inc. | 03/17/2022SE |
| K173807 | Accu O2 Oxygen AnalyzerCCL · Abbreviated | Precision Medical, Inc. | 05/02/2018SE |
| K153659 | MaxO2MECCL · Traditional | Maxtec, LLC | 06/10/2016SE |
| K123195 | Carescape Respiratory Modules, E-Sco, E-Scov, E-Scaiov and AccessoriesCCL · Traditional | GE Healthcare Finland Oy | 02/28/2013SE |
| K122290 | Envitec Mysign O Oxygen Measuring DeviceCCL · Traditional | Envitec-Wismar GmbH | 01/23/2013SE |
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| K801623 | Cavitron Ultrasonic Surg. Aspir. CusaLFL · Traditional | 11/18/1980SE |
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| K800722 | Auto-Field D Automated Visual DetectorHPT · Traditional | 04/29/1980SE |
| K791585 | Model G-61 Ultrasonic Dental UnitELC · Traditional | 09/19/1979SE |
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Questions and answers
When was Analyzer, Oxygen, Model OM-92 cleared by the FDA?
Analyzer, Oxygen, Model OM-92 (K771028) received a 510(k) decision of Substantially Equivalent on July 5, 1977, 26 days after the submission was received.
What is the product code of K771028?
The FDA product code is CCL – Analyzer, Gas, Oxygen, Gaseous-Phase, a Class II (moderate risk) device regulated under 21 CFR 868.1720.