FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ELD-ARONDAK CHAIR
K Number: K926054
·
Decision Mar 22, 1993
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
34
Applicant Total
1
Review Days
111
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Basic Information
- Device Name
- ELD-ARONDAK CHAIR
- K Number
- K926054
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3100
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Al'S Woodcraft, Inc.
- Date Received
- December 1, 1992
- Decision Date
- March 22, 1993
- Product Code
- INM
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| INM | Chair, With Casters | FDA class 1 | Physical Medicine |
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