MOISTAIR FLUID AIR TUBING SET— 510(k) K974561
Substantially EquivalentAmerican Medical Devices, Inc.
FDA 510(k) clearance K974561 for MOISTAIR FLUID AIR TUBING SET, Substantially Equivalent on 1998-02-19. Applicant: American Medical Devices, Inc.. Device class: 1.
Clearance details
- Applicant
- American Medical Devices, Inc.
- Product code
- Code KYG
- Device class
- Class 1
- Regulation
- 21 CFR 886.4360
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
Recent devices under product code KYG
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