Indego— 510(k) K171334
Substantially EquivalentParker Hannifin Corporation
FDA 510(k) clearance K171334 for Indego, Substantially Equivalent on 2017-09-08. Applicant: Parker Hannifin Corporation. Device class: 2.
Clearance details
- Applicant
- Parker Hannifin Corporation
- Product code
- Code PHL
- Device class
- Class 2
- Regulation
- 21 CFR 890.3480
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Macedonia, OH, US
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