ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE— 510(k) K102582
Substantially EquivalentDevon Medical, Inc.
FDA 510(k) clearance K102582 for ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE, Substantially Equivalent on 2010-10-07. Applicant: Devon Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Devon Medical, Inc.
- Product code
- Code JOW
- Device class
- Class 2
- Regulation
- 21 CFR 870.5800
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- King Of Prussia, PA, US
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