PULSE DOSE SERIES— 510(k) K961126
Substantially EquivalentDevilbiss Health Care, Inc.
FDA 510(k) clearance K961126 for PULSE DOSE SERIES, Substantially Equivalent on 1996-10-21. Applicant: Devilbiss Health Care, Inc.. Device class: 2.
Clearance details
- Applicant
- Devilbiss Health Care, 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
- Somerset, PA, US
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