FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CROSS-CHECKS
K Number: K951113
·
Decision Aug 19, 1996
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
22
Review Days
528
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Basic Information
- Device Name
- CROSS-CHECKS
- K Number
- K951113
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.2800
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Steritec Products Mfg Co, Inc.
- Date Received
- March 10, 1995
- Decision Date
- August 19, 1996
- Product Code
- LRT
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LRT | Indicator, Sterilization | FDA class 2 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LRT), ordered by most recent decision date.
TST CONTROL INTEGRATOR FOR STEAM STERILIZERS
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STERILIZATION INDICATOR FOR FLASH STERILIZATION
FDA 510(k)
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·General Hospital
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