FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PAD, EXAMINING TABLE
K Number: K801936
·
Decision Aug 27, 1980
Classifications
1
FEI Numbers
187
Registration Numbers
187
Same Product Code
2
Applicant Total
2
Review Days
15
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- PAD, EXAMINING TABLE
- K Number
- K801936
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6140
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Volunteer Blind Industries, Inc.
- Date Received
- August 12, 1980
- Decision Date
- August 27, 1980
- 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.
DMI SERIES 90 EXAMINATION TABLE
FDA 510(k)
FDA Class 1
·General Hospital
BED TRAY
FDA 510(k)
FDA Class 1
·General Hospital
Other Clearances by Volunteer Blind Industries, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K801935 | PAD, HOSPITAL STRETCHER | Aug 27, 1980 | Substantially Equivalent |