FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STURDY MANUAL RESUSCITATOR
K Number: K032596
·
Decision Aug 5, 2004
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
3
Review Days
349
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Basic Information
- Device Name
- STURDY MANUAL RESUSCITATOR
- K Number
- K032596
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5915
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Sturdy Industrial Co., Ltd.
- Date Received
- August 22, 2003
- Decision Date
- August 5, 2004
- Product Code
- BTM
- 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 |
|---|---|---|---|
| BTM | Ventilator, Emergency, Manual (Resuscitator) | FDA class 2 | Anesthesiology |
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