MAXI-USE O2 DEVICE— 510(k) K861325
Substantially EquivalentB & F Medical Products, Inc.
FDA 510(k) clearance K861325 for MAXI-USE O2 DEVICE, Substantially Equivalent on 1986-09-09. Applicant: B & F Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- B & F Medical Products, Inc.
- Product code
- Code NFB
- Device class
- Class 2
- Regulation
- 21 CFR 868.5905
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toledo, OH, US
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