FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SAFE-STRIPS
K Number: K880548
·
Decision Sep 29, 1988
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
2
Review Days
233
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Basic Information
- Device Name
- SAFE-STRIPS
- K Number
- K880548
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.2800
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Medstar, Inc.
- Date Received
- February 9, 1988
- Decision Date
- September 29, 1988
- Product Code
- JOJ
- 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 |
|---|---|---|---|
| JOJ | Indicator, Physical/Chemical Sterilization Process | FDA class 2 | General Hospital |
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Other Clearances by Medstar, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K921612 | INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 | Aug 18, 1992 | Substantially Equivalent |