FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SURGICAL INSTRUMENT TRAY
K Number: K944025
·
Decision Nov 22, 1994
Classifications
1
FEI Numbers
875
Registration Numbers
875
Same Product Code
75
Applicant Total
2
Review Days
97
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Basic Information
- Device Name
- SURGICAL INSTRUMENT TRAY
- K Number
- K944025
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Riley Medical, Inc.
- Date Received
- August 17, 1994
- Decision Date
- November 22, 1994
- Product Code
- FSM
- 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 |
|---|---|---|---|
| FSM | Tray, Surgical, Instrument | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FSM), ordered by most recent decision date.
INSTRUMENT TRAY LINER
FDA 510(k)
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·General, Plastic Surgery
SINGLE USE INSTRUMENT TRAY
FDA 510(k)
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ARTHROSCOPY TRAY
FDA 510(k)
FDA Class 1
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OPEN HEART TRAY
FDA 510(k)
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HEART CATH TRAY
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MAJOR BASIN TRAY
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Other Clearances by Riley Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K993535 | METAPAK MULTI-PURPOSE INSTRUMENT TRAY | Dec 7, 2001 | Substantially Equivalent |