MODIFIED MEMORY RETRACTOR ARM— 510(k) K895537
Substantially EquivalentMedical Equipment Development Co., Inc.
FDA 510(k) clearance K895537 for MODIFIED MEMORY RETRACTOR ARM, Substantially Equivalent on 1989-09-22. Applicant: Medical Equipment Development Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Equipment Development Co., 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
- Traditional
- Location
- Cinnaminson, NJ, US
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