ORTHO WRAP— 510(k) K830622
Substantially EquivalentFast Wrap Co., Inc.
FDA 510(k) clearance K830622 for ORTHO WRAP, Substantially Equivalent on 1983-06-20. Applicant: Fast Wrap Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Fast Wrap Co., Inc.
- Product code
- Code FQM
- Device class
- Class 1
- Regulation
- 21 CFR 880.5075
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.