CRANK FRAME RETRACTOR— 510(k) K882071
Substantially EquivalentKarlin Technology, Inc.
FDA 510(k) clearance K882071 for CRANK FRAME RETRACTOR, Substantially Equivalent on 1988-06-10. Applicant: Karlin Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Karlin Technology, 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
- Marina Del Rey, CA, US
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More clearances from Karlin Technology, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.