FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BETA-CAP II ADAPTER
K Number: K801680
·
Decision Aug 4, 1980
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
3
Applicant Total
164
Review Days
13
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Basic Information
- Device Name
- BETA-CAP II ADAPTER
- K Number
- K801680
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4200
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Quinton, Inc.
- Date Received
- July 22, 1980
- Decision Date
- August 4, 1980
- Product Code
- GCE
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GCE | Adaptor, Catheter | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
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