REFLUX BED— 510(k) K896256
Substantially EquivalentCozcon, Inc.
FDA 510(k) clearance K896256 for REFLUX BED, Substantially Equivalent on 1989-11-08. Applicant: Cozcon, Inc.. Device class: 1.
Clearance details
- Applicant
- Cozcon, Inc.
- Product code
- Code INW
- Device class
- Class 1
- Regulation
- 21 CFR 890.3750
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Colchester, CT, US
Recent devices under product code INW
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