FLUFF UNDERPAD TYPE UP1001— 510(k) K802740
Substantially EquivalentBio D Corp.
FDA 510(k) clearance K802740 for FLUFF UNDERPAD TYPE UP1001, Substantially Equivalent on 1980-12-10. Applicant: Bio D Corp.. Device class: 1.
Clearance details
- Applicant
- Bio D Corp.
- Product code
- Code KME
- Device class
- Class 1
- Regulation
- 21 CFR 880.6060
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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