CAPTUS 500— 510(k) K921428
Substantially EquivalentCapintec Instruments, Inc.
FDA 510(k) clearance K921428 for CAPTUS 500, Substantially Equivalent on 1992-05-28. Applicant: Capintec Instruments, Inc.. Device class: 1.
Clearance details
- Applicant
- Capintec Instruments, Inc.
- Product code
- Code IZD
- Device class
- Class 1
- Regulation
- 21 CFR 892.1320
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pittsburgh, PA, US
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