CUDDLE UP PILLOW— 510(k) K882544
Substantially EquivalentOhio Medical Instrument Co., Inc.
FDA 510(k) clearance K882544 for CUDDLE UP PILLOW, Substantially Equivalent on 1989-01-31. Applicant: Ohio Medical Instrument Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Ohio Medical Instrument Co., Inc.
- Product code
- Code FRP
- Device class
- Class 1
- Regulation
- 21 CFR 880.5680
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.