FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DELTA ROLLING SELF-LICKING WALKER
K Number: K792064
·
Decision Oct 30, 1979
Classifications
1
FEI Numbers
340
Registration Numbers
340
Same Product Code
13
Applicant Total
1
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
- DELTA ROLLING SELF-LICKING WALKER
- K Number
- K792064
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3825
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Staricat, Inc.
- Date Received
- October 15, 1979
- Decision Date
- October 30, 1979
- Product Code
- ITJ
- 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 |
|---|---|---|---|
| ITJ | Walker, Mechanical | FDA class 1 | Physical Medicine |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (ITJ), ordered by most recent decision date.
CHILD'S WALKER
FDA 510(k)
FDA Class 1
·Physical Medicine
UMBRELLA WALKER
FDA 510(k)
FDA Class 1
·Physical Medicine
WALK N ROLL
FDA 510(k)
FDA Class 1
·Physical Medicine
RESI-WALKER
FDA 510(k)
FDA Class 1
·Physical Medicine
RESI-WALKER
FDA 510(k)
FDA Class 1
·Physical Medicine
LIGHT WEIGHT ALUMINUM WALKER
FDA 510(k)
FDA Class 1
·Physical Medicine