FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
FUNNEL ADAPTOR
K Number: K923265
·
Decision Mar 18, 1993
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
56
Applicant Total
10
Review Days
259
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Basic Information
- Device Name
- FUNNEL ADAPTOR
- K Number
- K923265
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5880
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Southmedic, Inc.
- Date Received
- July 2, 1992
- Decision Date
- March 18, 1993
- Product Code
- CAD
- 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 |
|---|---|---|---|
| CAD | Vaporizer, Anesthesia, Non-Heated | FDA class 2 | Anesthesiology |
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| K101953 | SMDIA-1000 | Jan 7, 2011 | Substantially Equivalent |
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| K945993 | VAPOFIL | Feb 22, 1995 | Substantially Equivalent |
| K863318 | AEROSOL-T | Sep 11, 1986 | Substantially Equivalent |
| K861839 | VAPOFIL | May 21, 1986 | Substantially Equivalent |
| K860545 | VAPORIZER SPACER | Apr 17, 1986 | Substantially Equivalent |
| K843993 | ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 | Nov 15, 1984 | Substantially Equivalent |