PULSAR EM— 510(k) K882816
Substantially EquivalentApex Medical, Inc.
FDA 510(k) clearance K882816 for PULSAR EM, Substantially Equivalent on 1989-04-27. Applicant: Apex Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Apex Medical, Inc.
- Product code
- Code ILX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Martinsville, IN, US
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