CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L— 510(k) K003533
Substantially EquivalentSteritec Products, Inc.
FDA 510(k) clearance K003533 for CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L, Substantially Equivalent on 2001-02-07. Applicant: Steritec Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Steritec Products, Inc.
- Product code
- Code JOJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Castle Rock, CO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.