MASTEL LASER CLEAN ROOM, MODEL EBS-100— 510(k) K043494
Substantially EquivalentMastel Precision Surgical Instruments, Inc.
FDA 510(k) clearance K043494 for MASTEL LASER CLEAN ROOM, MODEL EBS-100, Substantially Equivalent on 2005-10-04. Applicant: Mastel Precision Surgical Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Mastel Precision Surgical Instruments, Inc.
- Product code
- Code FYD
- Device class
- Class 2
- Regulation
- 21 CFR 878.5070
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rapid City, SD, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.