FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DMI SERIES 90 EXAMINATION TABLE
K Number: K894788
·
Decision Sep 8, 1989
Classifications
1
FEI Numbers
187
Registration Numbers
187
Same Product Code
2
Applicant Total
4
Review Days
42
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Basic Information
- Device Name
- DMI SERIES 90 EXAMINATION TABLE
- K Number
- K894788
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6140
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- M.D. Intl., Inc.
- Date Received
- July 28, 1989
- Decision Date
- September 8, 1989
- Product Code
- KMN
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KMN | Chair And Table, Medical | FDA class 1 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KMN), ordered by most recent decision date.
PAD, EXAMINING TABLE
FDA 510(k)
FDA Class 1
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BED TRAY
FDA 510(k)
FDA Class 1
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