MEDI-JECTOR— 510(k) K772129
Substantially EquivalentDerata Corp.
FDA 510(k) clearance K772129 for MEDI-JECTOR, Substantially Equivalent on 1977-12-08. Applicant: Derata Corp.. Device class: 2.
Clearance details
- Applicant
- Derata Corp.
- Product code
- Code KZE
- Device class
- Class 2
- Regulation
- 21 CFR 880.5430
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Derata Corp.
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