STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234— 510(k) K001649
Substantially EquivalentSteritec Products, Inc.
FDA 510(k) clearance K001649 for STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234, Substantially Equivalent on 2000-06-23. 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.