FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL
K Number: K820574
·
Decision Mar 23, 1982
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
19
Applicant Total
3
Review Days
21
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Basic Information
- Device Name
- ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL
- K Number
- K820574
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4950
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- David Simmonds Co., Inc.
- Date Received
- March 2, 1982
- Decision Date
- March 23, 1982
- Product Code
- BWN
- 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 |
|---|---|---|---|
| BWN | Table And Attachments, Operating-Room | FDA class 1 | General, Plastic Surgery |
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