MODIFIED EXTERNAL PAD— 510(k) K891000
Substantially EquivalentInstromedix, Inc.
FDA 510(k) clearance K891000 for MODIFIED EXTERNAL PAD, Substantially Equivalent on 1989-05-19. Applicant: Instromedix, Inc.. Device class: 1.
Clearance details
- Applicant
- Instromedix, Inc.
- Product code
- Code DWS
- Device class
- Class 1
- Regulation
- 21 CFR 870.4500
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hillsboro, OR, US
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