FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF
K Number: K925744
·
Decision Jul 30, 1993
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
197
Applicant Total
17
Review Days
259
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Basic Information
- Device Name
- TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF
- K Number
- K925744
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1120
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Pymah Corp.
- Date Received
- November 13, 1992
- Decision Date
- July 30, 1993
- Product Code
- DXQ
- 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 |
|---|---|---|---|
| DXQ | Blood Pressure Cuff | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
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