A1 ACOUSTIC RHINOMETER— 510(k) K972140
Substantially EquivalentG.M. Instruments , Ltd.
FDA 510(k) clearance K972140 for A1 ACOUSTIC RHINOMETER, Substantially Equivalent on 1998-09-30. Applicant: G.M. Instruments , Ltd.. Device class: 2.
Clearance details
- Applicant
- G.M. Instruments , Ltd.
- Product code
- Code BXQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.1800
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kilwinning, GB
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Data sourced from openFDA. This site is unofficial and independent of the FDA.