FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRITIKON CENTRAL STATIN MONITOR
K Number: K933404
·
Decision Feb 9, 1994
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
51
Review Days
212
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Basic Information
- Device Name
- CRITIKON CENTRAL STATIN MONITOR
- K Number
- K933404
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Critikon Company, LLC
- Date Received
- July 12, 1993
- Decision Date
- February 9, 1994
- Product Code
- DPS
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DPS | Electrocardiograph | FDA class 2 | Cardiovascular |
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| K982342 | DINAMAP MPS SELECT PORTABLE MONITOR | Aug 14, 1998 | Substantially Equivalent |
| K943709 | DINAMAP PLUS VITAL SIGNS MONOITOR | Jun 16, 1995 | Substantially Equivalent |
| K942700 | DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340 | Mar 1, 1995 | Substantially Equivalent |
| K933050 | CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH | Dec 14, 1993 | Substantially Equivalent |
| K915697 | CRITIKON VITAL SIGNS MODULE | Jul 1, 1993 | Substantially Equivalent |
| K921295 | INTRAVENOUS CATHETERS MODIFICATIONS | May 17, 1993 | Substantially Equivalent |
| K912188 | DINAMAP PLUS PHYSIOLOGICAL MONITOR MODEL 8700 | Dec 4, 1991 | Substantially Equivalent |