INSTRUMED RETRACTORS— 510(k) K071771
Substantially EquivalentInstrumed International, Inc.
FDA 510(k) clearance K071771 for INSTRUMED RETRACTORS, Substantially Equivalent on 2007-08-02. Applicant: Instrumed International, Inc.. Device class: 2.
Clearance details
- Applicant
- Instrumed International, Inc.
- Product code
- Code GZT
- Device class
- Class 2
- Regulation
- 21 CFR 882.4800
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Schaumburg, IL, US
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More clearances from Instrumed International, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.