FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TECHTON PROTECTIVE PAD
K Number: K873038
·
Decision Apr 3, 1989
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
2
Applicant Total
1
Review Days
608
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
- TECHTON PROTECTIVE PAD
- K Number
- K873038
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.6500
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Techton, Inc.
- Date Received
- August 4, 1987
- Decision Date
- April 3, 1989
- Product Code
- IWQ
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IWQ | Curtain, Protective, Radiographic | FDA class 1 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IWQ), ordered by most recent decision date.
MAVIG LOWER BODY PROTECTION SYSTEMS, ASSEMBLY MODELS 6265, 6266, 6267, 6268, 6269/0, 629/1, AND 6269/2
FDA 510(k)
FDA Class 1
·Radiology
X-RAY DRAPES
FDA 510(k)
FDA Class 1
·Radiology