FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FACE-IT SHIELD
K Number: K942022
·
Decision Jul 8, 1994
Classifications
1
FEI Numbers
801
Registration Numbers
801
Same Product Code
55
Applicant Total
47
Review Days
73
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Basic Information
- Device Name
- FACE-IT SHIELD
- K Number
- K942022
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4040
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Onyx Medical Corp.
- Date Received
- April 26, 1994
- Decision Date
- July 8, 1994
- Product Code
- LYU
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| LYU | Accessory, Surgical Apparel | FDA class 1 | General, Plastic Surgery |
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Other Clearances by Onyx Medical Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K931690 | SPOON PLATE | Jun 7, 1994 | Substantially Equivalent for Some Indications |
| K934614 | MINI FRAGMENT PLATE | May 4, 1994 | Substantially Equivalent for Some Indications |
| K931692 | T-PLATE | May 4, 1994 | Substantially Equivalent for Some Indications |
| K931684 | EPIPHYSIS PLATE | May 4, 1994 | Substantially Equivalent for Some Indications |
| K931680 | CANNULATED CANCELLOUS SCREW | May 4, 1994 | Substantially Equivalent for Some Indications |
| K931679 | BUTTRESS PLATE | Apr 25, 1994 | Substantially Equivalent for Some Indications |
| K934615 | CANCELLOUS BONE SCREW | Apr 25, 1994 | Substantially Equivalent for Some Indications |
| K931683 | CLOVERLEAF PLATE | Apr 25, 1994 | Substantially Equivalent for Some Indications |
| K931693 | 1/3 TUBULAR PLATE | Apr 25, 1994 | Substantially Equivalent for Some Indications |
| K931687 | MULTIPLE FRAGMENT PLATE | Apr 25, 1994 | Substantially Equivalent for Some Indications |