SPINAL NEEDLE— 510(k) K960405
Substantially EquivalentPromex, Inc.
FDA 510(k) clearance K960405 for SPINAL NEEDLE, Substantially Equivalent on 1996-02-28. Applicant: Promex, Inc.. Device class: 2.
Clearance details
- Applicant
- Promex, Inc.
- Product code
- Code MIA
- Device class
- Class 2
- Regulation
- 21 CFR 868.5150
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
Recent devices under product code MIA
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More clearances from Promex, Inc.
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