FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ULTRABRONZ SERIES 800 (ECLIPSE) TANNING BED
K Number: K931661
·
Decision Dec 17, 1993
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
80
Applicant Total
2
Review Days
256
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Basic Information
- Device Name
- ULTRABRONZ SERIES 800 (ECLIPSE) TANNING BED
- K Number
- K931661
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4635
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Eurocut, Ltd.
- Date Received
- April 5, 1993
- Decision Date
- December 17, 1993
- Product Code
- LEJ
- 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 |
|---|---|---|---|
| LEJ | Booth, Sun Tan | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Eurocut, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K931660 | ULTRABRONZ SERIES 400 TANNING BED | Dec 17, 1993 | Substantially Equivalent |