FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
STETSKINS
K Number: K930118
·
Decision Mar 26, 1993
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
2
Applicant Total
1
Review Days
74
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Basic Information
- Device Name
- STETSKINS
- K Number
- K930118
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.1930
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Nova Diversified Concepts
- Date Received
- January 11, 1993
- Decision Date
- March 26, 1993
- Product Code
- BZS
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| BZS | Stethoscope Head | FDA class 1 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BZS), ordered by most recent decision date.
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