ARP RX100— 510(k) K093259
Substantially EquivalentArp Manufacturing, Inc.
FDA 510(k) clearance K093259 for ARP RX100, Substantially Equivalent on 2009-12-17. Applicant: Arp Manufacturing, Inc.. Device class: 2.
Clearance details
- Applicant
- Arp Manufacturing, Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boulder, CO, US
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