FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SPIROMED 2
K Number: K851620
·
Decision May 10, 1985
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
226
Applicant Total
78
Review Days
22
Basic Information
- Device Name
- SPIROMED 2
- K Number
- K851620
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.1840
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- DRAEGER MEDICAL, INC.
- Date Received
- April 18, 1985
- Decision Date
- May 10, 1985
- Product Code
- BZG
- 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 |
|---|---|---|---|
| BZG | Spirometer, Diagnostic | FDA class 2 | Anesthesiology |
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| K041622 | MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM | Jul 8, 2004 | Substantially Equivalent |
| K040847 | MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR | Jun 17, 2004 | Substantially Equivalent |
| K033498 | NARKOMED 6400, MODEL NM6400 | Apr 26, 2004 | Substantially Equivalent |
| K030624 | MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM | Mar 17, 2004 | Substantially Equivalent |
| K031400 | FABIUS TIRO ANESTHESIA SYSTEM | Jul 15, 2003 | Substantially Equivalent |
| K022031 | NARKOMED MRI-2 ANESTHESIA SYSTEM, MODEL NM-MRI-2 | Aug 29, 2002 | Substantially Equivalent |