MEGA GENERAL PURPOSE INSTRUMENT KIT— 510(k) K910366
Substantially EquivalentMegadyne Medical Products, Inc.
FDA 510(k) clearance K910366 for MEGA GENERAL PURPOSE INSTRUMENT KIT, Substantially Equivalent on 1991-03-28. Applicant: Megadyne Medical Products, Inc.. Device class: 1.
Clearance details
- Applicant
- Megadyne Medical Products, Inc.
- Product code
- Code KDD
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hauppauge, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.