OK Plus Indicator— 510(k) K222137
Substantially EquivalentPropper Manufacturing Co., Inc.
FDA 510(k) clearance K222137 for OK Plus Indicator, Substantially Equivalent on 2022-12-05. Applicant: Propper Manufacturing Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Propper Manufacturing Co., Inc.
- Product code
- Code JOJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Long Island, NY, US
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