RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP— 510(k) K960591
Substantially EquivalentChalgren Enterprises, Inc.
FDA 510(k) clearance K960591 for RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP, Substantially Equivalent on 1996-06-13. Applicant: Chalgren Enterprises, Inc.. Device class: 2.
Clearance details
- Applicant
- Chalgren Enterprises, Inc.
- Product code
- Code IKT
- Device class
- Class 2
- Regulation
- 21 CFR 890.1385
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gilroy, CA, US
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