FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIOPACK
K Number: K993685
·
Decision Jul 18, 2000
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
3
Review Days
260
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Basic Information
- Device Name
- BIOPACK
- K Number
- K993685
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5500
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Bioscan, Inc.
- Date Received
- November 1, 1999
- Decision Date
- July 18, 2000
- Product Code
- ILY
- 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 |
|---|---|---|---|
| ILY | Lamp, Infrared, Therapeutic Heating | FDA class 2 | Physical Medicine |
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