FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TABLE, OPERATING, FIELD 6530-00-709-8175
K Number: K821923
·
Decision Jul 13, 1982
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
2
Applicant Total
4
Review Days
14
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
- TABLE, OPERATING, FIELD 6530-00-709-8175
- K Number
- K821923
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4950
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Emerson-Sack-Warner Corp.
- Date Received
- June 29, 1982
- Decision Date
- July 13, 1982
- Product Code
- FWX
- 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 |
|---|---|---|---|
| FWX | Table, Operating-Room, Mechanical | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FWX), ordered by most recent decision date.
ALM OPERATING TABLES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MOBILE OPHTHALMIC OPERATING TABLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery